262 open positions
HQI 78
Are you driven by high standards, consistency, and making learning truly effective? Join us as a Learning and Quality Assurance Lead to play a critical role in strengthening training quality and delivery standards across Elysium Healthcare. In this role, you will be the custodian of training capability across the organisation click apply for full job details
HQI 83
Company Description At Turner & Townsend we’re passionate about making the difference. That means delivering better outcomes for our clients, helping our people to realize their potential, and doing our part to create a prosperous society.  Every day we help our major Pharmaceutical clients deliver ambitious and highly technical projects worldwide. Are you interested in working for the world’s leading pharma corporations, delivering their world class, large scale complex projects?  Job Description We are seeking a QA/QC professional with a comprehensive vision, a strong sense of responsibility, and proven technical experience in industrial civil, structural, and architectural (CSA) projects . This role is critical to ensuring that construction processes meet the highest quality standards and applicable regulations, delivering complete, safe, and contract-compliant outcomes. Qualifications Key Responsibilities: • Develop and implement quality assurance and control plans in accordance with national and international standards (NOM, ASTM, ACI, AISC, AWS). • Verify materials, construction procedures, inspection protocols, and site records for civil, structural, and architectural works. • Conduct daily technical inspections and generate photographic and documentary reports. • Initiate and manage Non-Conformance Reports (NCRs) and coordinate corrective actions. • Oversee the execution of technical inspections and testing activities for soil compaction, concrete, structural steel, welding, coatings, and architectural finishes. • Participate actively in progress meetings and present technical and quality updates at the executive level. • Coordinate the technical and documentary closeout of projects. • Collaborate with planning, supervision, and PMO teams to ensure timely and complete deliverables. • Represent the company in audits, inspections, or client and regulatory reviews Requirements: • Minimum of 5 years of proven experience as QA/QC in industrial projects, particularly in civil, structural, and architectural works for power, energy, or industrial facilities. • In-depth knowledge of quality standards and construction codes applicable to the Colombian market. • Strong skills in documentation, record control, and executive-level reporting. • Bilingual in Spanish and English, both written and spoken. • Ability to perform under pressure with a results-driven mindset. • Structured, organized, self-motivated, and capable of resolving complex technical issues. Preferred Qualifications: • Certifications in QA/QC, ISO 9001, or related fields. • Experience with digital quality control tools and collaborative platforms. • Background or training in LEAN Construction, Scrum, or other agile methodologies. • Previous experience with industrial energy, EPC, or CFE-related projects   Additional Information Our inspired people share our vision and mission. We provide a great place to work, where each person has the opportunity and voice to affect change. We want our people to succeed both in work and life. To support this we promote a healthy, productive and flexible working environment that respects work-life balance.  Turner & Townsend is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and actively encourage applications from all sectors of the community. Please find out more about us at  www.turnerandtownsend.com/ #LI-LP1 Join our social media conversations for more information about Turner & Townsend and our exciting future projects:  Twitter Instagram LinkedIn It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time.  Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review. 
HQI 83
Company Description Wise is a global technology company, building the best way to move and manage the world’s money. Min fees. Max ease. Full speed. Whether people and businesses are sending money to another country, spending abroad, or making and receiving international payments, Wise is on a mission to make their lives easier and save them money. As part of our team, you will be helping us create an entirely new network for the world's money. For everyone, everywhere. More about our mission and what we offer . Job Description As a Quality Assurance Specialist with a focus on SAR Reporting at Wise, you are responsible for providing expert, objective assurance on the quality and effectiveness of our operational processes and controls. Your core function is to ensure risks are identified, assessed and mitigated in line with policy requirements, and to identify weaknesses, assess risk materiality and report outcomes. You will apply your risk expertise and critical thinking to conduct holistic and detailed reviews in line with agreed methodologies and KPIs, and make recommendations to drive continuous improvement. This role plays an integral part in helping Wise achieve its mission of Money WIthout Borders, through effective and value-add assurance. This is a role for specialist who has had experience with external suspicious activity reporting, regulatory compliance and FIUs. Activities performed on the job • Conduct holistic, risk-based reviews using test scripts and scorecards to assess risk outcomes, compliance with global and regional policies, relevant guidance and risk appetite.  • Assess risk, materiality and root causes for each finding, providing clear and robust reasons aligned to policy compliance and/or risk mitigation.  • Participate in calibration exercises to share findings, best practice and ensure consistent, correct decisions are made across the team.  • Clearly communicate outcomes to stakeholders covering key risks, issues, root causes, and recommendations, maintaining robust records and audit trails.   • Analyse, assess and communicate emerging themes and trends, recommending opportunities for continuous improvement.  • When assigned, scope, plan, and execute root cause analysis or targeted investigations. • Contributes to team collaboration and knowledge sharing to enhance team capabilities. • Take a proactive approach to consistently achieving individual and team targets (KPIs, SLAs), demonstrating a strong commitment to both quality and speed. Meet deadlines, optimise processing times and take full ownership and accountability to deliver results.  • Perform additional tasks as assigned by your lead, demonstrating adaptability and a proactive approach. This includes actively participating in meetings, training, and internal events to support broader team and company objectives. • Embody and uphold Wise’s values in daily interactions. Qualifications Required Skills:  • Professional experience: 2+ years of experience in QA related to BSA/AML or experience in AML Investigations or SAR Reporting • Fluent in English (written and verbal skills) with the ability to clearly articulate your thoughts and recommendations. • Self-Development: Takes ownership for personal development, including commitment to develop expertise through industry and trend analysis, regulatory insights, and emerging risk typologies.  Functional Skills:  • Quality Assurance methodology: Good understanding of Quality Assurance methodologies and frameworks, including testing procedures, scoring criteria and root cause analysis. Applies consistent standards across all reviews.  • Risk and Compliance expertise relevant to SAR Reporting, including the ability to identify and assess risks, interpret and apply policy requirements and guidance, and a good understanding of the regulatory environment applicable to the function.  • Analytical Skills: Efficient at reviewing and investigating customer files, identifying missing information, issues, trends and root causes, using AI and data as appropriate.  • Systems and Tools: Competent using case management systems, dashboards, AI tools to support case working and analysis. Understands automation, AI, and is comfortable working with evolving tools and technologies to enhance ways of working.  Behavioural  Skills: • Critical thinking: Ability to critically assess information, demonstrate attention to detail, challenge assumptions, dig deeper where required, ask the right questions and connect data across different sources to make informed and risk-based decisions, explaining your rationale to ensure our QA outcomes can withstand audit and regulatory scrutiny.  • Risk management: Uses facts, data, policy and risk frameworks to support conclusions and assess risk materiality ensuring decisions can be justified.  • Documentation and communication skills: Clear, constructive and concise written and verbal skills, with ability to explain risks and issues in simple terms in a constructive and actionable manner. • Adaptability: Able to keep up with evolving requirements and ongoing changes impacting QA team, policy, guidance, processes and systems. Open to feedback and continuous improvement.  Effective expectations and KPIs • Dynamic KPIs and expectations ensure that the metrics used to evaluate performance remain relevant and aligned with the goals and circumstances of the team and the individual. This flexibility helps both the organisation and employees adapt to change and continuously improve. • The KPIs and effective expectations are designed to measure effectiveness, productivity, and overall contribution to team and company objectives, while also setting clear behavioural standards for the assigned role. KPIs and expectations are dynamic and will be shared with you for your role and team. Additional Information For everyone, everywhere. We're people building money without borders  — without judgement or prejudice, too. We believe teams are strongest when they are diverse, equitable and inclusive. We're proud to have a truly international team, and we celebrate our differences. Inclusive teams help us live our values and make sure every Wiser feels respected, empowered to contribute towards our mission and able to progress in their careers. If you want to find out more about what it's like to work at Wise visit  Wise.Jobs . Keep up to date with life at Wise by following us on  LinkedIn  and  Instagram .
HQI 83
Company Description We’re the nation’s favourite heating brand, here to warm up people’s homes, lives, and futures.   From boilers, hybrids and heat pumps to solar thermal and smart controls, we’re giving our customers plenty of choice. With cutting-edge tech and research, we’re right in the thick of the drive for a better future of home heating.   It’s not all tools and tech. People are the real heart of our company. We connect with our customers to deliver genuinely helpful support, and we care about our employees and give them enriching careers. We work hard, we work together, and we work with a cause – delivering brilliant customer support and exceptional engineering.   As an organisation of more than 1,600 employees, we also take our role in the communities we serve seriously. From giving away free heating systems for community spaces, to our charity, education, and volunteer work – we’re no strangers to rolling our sleeves up, getting stuck in, and helping out.   If that sounds like something you’d like to be a part of, we’d love to meet you.   Come and work #LikeABosch at Worcester Bosch.   Job Description Your Purpose: • Support the Purchasing Quality Assurance team in their day-to-day activities. • Work with a national and international Purchasing Quality team and support the business of Home Comfort in developing the supply base. Role Scope: • Support the Purchasing Quality Assurance team in dealing with quality topics from purchased parts. • Support the problem solving and investigation of internal component complaints. • Dealing with internal and external cross departmental teams. • Dealing with external suppliers as required. • Support the returns to supplier & cost collection process. • Support the data management of quality complaints and supplier data. • General administrative work when required. Key Focuses: • Support Production dealing with quality issues of purchased components. • Containment actions and problem-solving activities. • Inspection of delivered goods. • Returns to suppliers & reimbursement process. • Supplier data management in SAP. Additional Information about the role: • Provide technical support to production and other departments regarding non-conformances. • Analysis, update and development of Purchase Quality databases as necessary. • Participate in the Continuous Improvement Process. • Other general projects or quality engineering duties as required. Qualifications • Be the type of person people like interacting with, this role relies on great working relationships! • Very good communication and networking skills. • Determined and resilient, able to deal with challenges and find solutions. Attention to detail. • Possess strong analytical skills and critical thinking. • Be hands-on and have an agile mindset. • Proficient skills in MS Excel as a starting point, with experience / knowledge of more office and software applications. • Be target orientated, and able to meet deadlines. • Forward thinking, with strong organisational skills. • Proactive and self-motivated, able to work independently. • A University (academic) education, and studies in Engineering are a must to this role preferably HND or BEng in Mechanical or Manufacturing Engineering. Additional Information Deadline for Applications: Please note, we reserve the right to close this vacancy at any time so we encourage candidates to submit their applications as soon as possible.   Working Hours: 39 hours per week – standard working pattern of 08:00 – 17:00 Monday to Thursday and 08:00 – 16:00 Friday with a 1-hour lunch break  Working with us comes with the following benefits:  • Office based role  • 25 days annual leave per year plus bank holidays (pro-rata for your first year)  • Eligibility for our Company Performance Bonus (up to £2,000 gross per annum)  • Enhanced pension contributions  • Access to the Perkbox and My Benefits platforms giving access to discounts, group income protection and death in service benefits  • Employee Assistance Programme and Virtual GP  • Discounts on products from across the Bosch Group  • Subsidised on-site café and canteen  • Health & well-being support including: over 200 trained mental health first aid champions  • Access to Bosch Social Club membership offering you and up to 5 friends and family discounts on excursions and events  • Volunteering days  • Policy to support growing families  • Access to self-service training platform containing over 200 Bosch approved programmes  • Networking opportunities across Bosch UK including a mentoring programme  • And more!
HQI 82
🚀 Challenge the Impossible About Beyond Gravity Beyond Gravity, headquartered in Zurich, Switzerland, is the first space company to combine a startup mindset, agility, speed and innovation with decades of experience and proven quality. Approximately 1800 employees at 12 locations in six countries (Switzerland, Sweden, Austria, USA, Finland and Portugal) develop and manufacture products for satellites and launch vehicles with the goal of advancing humankind and enabling the exploration of the world and beyond. Beyond Gravity is the preferred supplier of structures for all types of launch vehicles and a leading provider of selected satellite products and constellation solutions in the New Space sector. In 2024, the company generated a revenue of around CHF 359 million. More information at: www.beyondgravity.com Your crew We are a team of more than 10 professionals. Our expertise includes product assurance, managing product project quality from customer quotation to project closure, as well as quality assurance, ensuring that our manufacturing quality meets the agreed-upon criteria. We ensure that the high level of quality demanded by our international customers is always achieved for our space products. The entire department has a very diverse structure in terms of age, experience, knowledge, education and nationalities. We are proud of the strong team spirit in our department, warmly welcome new members and prioritize the training of new employees. Your mission Responsibilities: Develop the Quality Assurance Requirements and Culture, ensuring robust quality processes, cost excellence for program quality execution through collaboration with engineering, operations and supply chain. Act as main interface for Process Engineering and Operations for all quality and safety topics Establish Critical-to-Quality (CTQ) features in collaboration with Process Engineering and Operations Lead Non-Conformance and failure investigation whenever product and/or process requirements are violated Supervise and direct Internal Manufacturing Assembly Integration and Test (MAIT) Process Development and Qualification for all relevant quality aspects Perform Key Inspection Point (KIP) and Mandatory Inspection Point (MIP) Documentation (Production Records) to verify Critical Features/Requirements Main Tasks: Execute Quality Assurance Program in accordance with Project Milestones Ensure successful execution of the Customer, Regulatory and Internal Requirements for Operations Execution Convert the Customer Critical to Quality Requirements into internal specifications and requirements Lead and coordinate the Internal Process for Non-Conformance Management Lead Operations Critical Root Cause Analysis (RCA) and investigation activities Moderate Process FMEA Develop Process Critical-to-Quality (CTQ) and Control Plans in collaboration with Process Engineering and Operations Establish Process Quality Documentation Support Process Qualification Contribute for Quality matters to proposal as part of the Request For Information / Request For Quotation Contribute as needed to Customer and Internal Audit as Quality Assurance representative. Contribute to the Quality Organization Development (Training/Coaching) Most important output: Contribute to Customer Satisfaction for Quality Performance Operations Quality Performance Process FMEA Process Critical-to-Quality (CTQs) and Control Plans Input to the Product Quality data-package for Space Application Input to the Final Product Qualification data-package for Space Application Internal Root Cause Analysis and Non-Conformance Report Your story Must's: Relevant experience in the field of Quality and Continuous Improvement Preferred education: BSc/MSc degree in Engineering or in a similar relevant discipline Knowledge of standards such as EN9100, ECSS, NASA and MIL Ability to quickly understand and analyze technical products/systems and their function High level of theoretical skills in relevant fields with an adeptness to coach hands on practical elements “on the floor” Excellent written and oral communication skills in English MS Office experience required Experience in the application of Quality preventive methodology (5Why, Ishikawa Fishbone…) Nice to have: Any further language (German, French and Swedish) beyond English is a strong asset Experience in other Space companies Why Beyond Gravity To work in a growing high technology company with career opportunities within the site or internationally. You will be a part of an engaged team with the ambition to innovate space! We offer a hybrid work situation, high flexibility and autonomy, and a great team to develop and have fun with! 🌌Are you ready for lift-off? Our core values - Passionate, Together, and Curious - transform challenges into opportunities. Embark on a journey to transcend the ordinary with us. We‘re actively reviewing candidates and will promptly select the ideal fit for our team. For questions regarding the recruitment process, please contact: Breno Silva | breno.silva@beyondgravity.com Beyond Gravity is proud to be an Equal Opportunity Employer. We welcome and encourage applications from all qualified individuals, regardless of race, color, religion, sex, gender, national origin, disability, protected veteran status, or any other legally protected categories. Applications by e-mail cannot be considered. We do not accept dossiers from recruitment agencies for this position.
HQI 75
Mō te tūnga | About the role Joint Support Group (JSG) provides multifunctional health services to the New Zealand Defence Force personnel both within New Zealand and overseas in support of all NZDF outputs. The purpose of this position is to develop, lead and manage risk, together with quality and improvement for JSG. Other key responsibilities are: * Responsible for identifying and leading in collaboration with DHO and FHO improvements in service delivery to support JSG developing an integrated and holistic health service to all military personnel in NZDF. * Development and monitoring of health services performance and risk management systems and processes. * Work with the FHO and DHO Quality and Clinical Advisors to provide subject matter expertise and support. * Build and maintain positive working relationships with internal stakeholders continually maintaining “customer first” mindset. * Undertake organisational performance reporting against agreed goals and objectives. The salary for this role ranges from $104,214 - $115,131, inclusive of a 4% superannuation contribution. Appointments within this range are based on skills and experience. Ngā pūkenga me ngā wheako | Skills and Experience To be successful in this role you will need: * Extensive experience in Quality Assurance and Improvement (5 or more years' experience) in the health sector. * Sound knowledge of clinical practice, health management processes and systems. * Sound knowledge of NZ health legislation and compliance relating to the provision of health services. * Sound knowledge of risk management and practices, and * In-depth experience of quality improvement and assurance systems, tools and processes. You will also be a confident communicator, be engaging with your stakeholders and teams you work alongside and be customer service centric. This role requires occasional domestic travel throughout New Zealand; you will need to have no issues with travel and have a clean Class 1 Full Driver's Licence. Nōu te rourou | What's in it for you Your skills and dedication deserve recognition, and NZDF delivers with competitive pay matched to your experience. But that's just the beginning – safeguard your loved ones with a fully funded life cover of up to $300,000 and critical illness protection. Other benefits include discounted additional insurances, free will services and savings schemes for the Defence community. Get expert financial guidance and mortgage broker services. Find all our benefits and more on the Force 4 Families website. NZDF champions diversity and inclusivity, valuing every member and fuelling their success. We embrace uniqueness, understanding that diverse teams drive creativity, innovation, and excellence. With an open door to all – irrespective of gender, ethnicity, ability, age, or family dynamics – NZDF offers a flexible, empowering work environment. Join us in shaping a brighter future, where everyone thrives. Me pēhea te tuku tono | How to Apply Applications close on Monday 26 October 2026. Use the links on this page where you'll be directed to the Defence Careers website. Please Note: * All applications must be made online, via the Defence Careers website. Each listing contains the Position Description and a Contact Us option for any queries or technical issues. * Your cover letter will be a key part of our selection process, so please highlight how your experience relates to the key activities outlined in the Advert and Position Description. * Applicants will be required to undergo a pre-employment drug-screening test prior to any offer of employment being made. NZDF Employees/Members – please apply internally via the HR Toolkit; this will ensure that you are visible as an internal candidate. NZDF Contractors – please apply via the Defence Careers website. NZDF Reserves – please apply via the Defence Careers website if you cannot access the HR Toolkit. NZDF is currently undertaking a Workforce Savings Programme (WSP) to realise efficiencies and required enduring savings, in which NZDF has proposed some changes to the organisational structure of its civilian workforce. At this point in time this position is proposed to be impacted by a minor change in reporting line. Please Note: To be eligible for the required level of government security clearance with the NZ Defence Force, you need to meet certain citizenship and residency criteria. Here's what you need to know: Low Level Security Clearance * You must be a New Zealand citizen or you must hold New Zealand Permanent Residence or have a current New Zealand Residency Class Visa. * At minimum, you must hold New Zealand Permanent Residence or have a current New Zealand Residency Class Visa, and you must be a citizen of and have lived in Australia, Canada, United Kingdom, United States of America or New Zealand continuously for the last five (5) years. * You must have a five (5) year background history that can be verified and assessed appropriately by the NZ Security Intelligence Service (NZSIS) to determine if you are suitable for a security clearance at this level. If you do not meet the minimum criteria, unfortunately, your application will not be accepted. We do welcome your application at a time when you will meet the requirements.
HQI 83
Career Category Quality Job Description Join Amgen's Mission to Serve Patients At Amgen, our shared mission to serve patients living with serious illnesses drives everything we do. Every team member plays an important role in helping advance science and deliver medicines that make a meaningful difference for patients around the world. Amgen fights the world's toughest diseases by harnessing the best of biology and technology. We draw on our scientific expertise to push beyond what is known today and help people live longer, fuller lives. If you are energized by collaboration, continuous learning, and meaningful work, we invite you to join our team and help make an impact. Specialist Quality Assurance I What you will do Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support Facilities & Engineering (F&E), Quality Control (QC), Technology, Process Development (PD) or Validation (all non-direct manufacturing areas) for the Biologics and Synthetic Manufacturing plants. Main Responsibilities : • Provide quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning and qualification, regulatory approval and market supply • Support routine GMP documentation review activities (e.g. SOPs, logbooks, work orders, validation documents, periodic reviews) and ensure key performance indicator met targeted metrics • Co-lead and support the deployment of Amgen quality systems, including management review, validation, deviation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations • Review and approve deviations, investigations, testing result investigations, change controls, and other quality records (with focus on highly complex records). Participate in and lead complex root cause investigations for deviations • Lead Quality Assurance oversight in commissioning and qualification projects or New Product Introduction (NPI) • Coach site Quality Assurance professionals on resolution of quality issues • Participate in regulatory inspections and interact directly with regulatory inspectors • Lead or support function/site/network initiatives and continuous improvement projects What we expect of you • Doctorate Degree • Master’s degree and 2 years of experience in pharmaceutical company or GMP environment OR • Bachelor’s degree and 4 years of experience in pharmaceutical company or GMP environment OR • Diploma and 8 years of experience in pharmaceutical company or GMP environment • Preferred 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems. • Direct experience with bulk manufacturing of biopharmaceuticals/API preferred. • Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff. People and stakeholder management. • Experience with regulatory audits and inspections· • Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality. Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company. What you can expect of us As we work to develop medicines for patients, we also invest in our people. Through competitive benefits, development opportunities, and a collaborative culture, we'll support your growth both professionally and personally. Apply now and help transform the lives of patients while transforming your career. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values as we continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation .
HQI 83
职位的任职者将 • 提供质量支持以实现 pMDI 项目里程碑。 • 确保青岛pMDI 项目计划在设计、施工、启动、验证（整个生命周期）期间符合 GMP 要求。 • 确保自有业务中验证计划的 GMP 合规性和运营有效性 • 与运营和质量部门的内部和外部同事进行跨职能互动，以确保完全符合 AZ 标准和当地法规。 • 支持 QA 和其他工程/运营人员以及相关技术科目的实习生，是 GMP 培训活动的主要贡献者。 • 与AZ 总部或跨职能部门合作，确保全球项目或青岛数字化、自主化项目的落地 • 根据需要支持监督和监督承包商和实习生活动 The role incumbent will • Provide Quality support to achieve the pMDI project milestones. • Ensuring compliance with GMP requirements during the design, construction, start-up,validation (entire life cycle) of Qingdao capital project initiative. • Ensuring GMP compliance and operational effectiveness of the validation program within owning business. • Cross functional interaction with both internal and external colleagues in Operations and Quality to ensure full compliance with AZ standards and local regulations. • Support QA and other engineering / operations staff and interns in relevant technical subjects and is a key contributor to GMP training activities. • Collaborate with AZ headquarters or cross-functional departments to ensure the implementation of global projects or Qingdao digitalization and autonomy projects. • Support the supervise and oversight contractors and intern activities as required. 职责（包括关键结果领域、具体责任、任务等） Job Responsibilities (to include key result, areas, specific accountabilities, tasks, etc.) • 为项目和工厂提供质量支持。 • 支持 GPQS、ECMS、GVLMS 数据库的开发。 • 参与青岛供应基地内 QMS 的建立，包括验证、变更控制、偏差和相关基础设施活动。 与pMDI 项目的工程 IT、QC、制造和技术功能进行对接，并在项目的设计、施工和启动阶段主动确保符合 GMP。 • 开发和推动必要的部门流程、文档和培训。 • 开发和维护技术能力，并与工程、IT、QC、制造和技术职能部门的同行合作。 • 支持 GMP 相关设施和设备系统的质量保证工作，以确保完全符合 GMP。 • 参加GMP 培训，严格遵守GMP 与法规要求 • 发展各种工作技能并追求持续的改进，参与并支持数字化和自主化项目。 • 根据业务需要完成安排的其他工作 • Provide quality support to the project and later site. • Support development of GPQS, ECMS, GVLMS database. • Participated in the building up of QMS including validation, change controls, deviations, and related infrastructure activities within the Qingdao Operations site. • Interface with engineering IT, QC, manufacturing, and technical functions on capital projects and proactively ensure GMP compliance during the design, construction and start up phases of the project. • Develop and drive necessary departmental process, documentation, and training. • Develops and maintains technical competency and collaborates with counterparts in engineering, IT, QC, manufacturing, and technical functions. • Supports quality assurance efforts for GMP related facility and equipment systems to ensure full GMP compliance. • Participate in GMP training and strictly comply with GMP and regulatory requirements. • Develop various work skills and pursue continuous improvement, participate in and support digital, and autonomous projects. • Complete other work assigned according to business needs. 教育、资历、技能和经验 Education, Qualifications, Skills and Experience 必备条件Essential 优先条件Desirable • 拥有学士学位，并具备药品质量、制造、技术的一般经验。 • 具备 cGMP 和全球 GMP 要求、质量体系 以及药品/设备测试技术和药典的充分知识。 • 具备计算机验证和21 CFR 11的基本知识。 • 具备良好的人际交往和解决问题的能力。 • 具备独立和协作处理多学科和多功能工作的能力。 • 使用中文和英文作为工作语言。 • 具备出色的口头和书面沟通能力，能够与 组织各个级别的人员进行有效沟通。 • Bachelor’s degree and general experience in pharmaceutical quality, manufacturing, or technical roles. • A good knowledge of cGMPs and global GMP requirements, quality systems, and pharmaceutical product/device testing technology and pharmacopeia. Well -developed interpersonal and problem solving skills. • A basic knowledge of computer validation requirements and 21 CFR 11 requirements. • Demonstrated ability to work independently and collaboratively on multidisciplinary and multifunctional. • Use both Chinese and English as working language. • Excellent oral and written communication skills with the ability to communicate effectively with individuals from all levels of the organization. Date Posted 22-10月-2026 Closing Date 30-12月-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
HQI 86
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Role When you are part of Thermo Fisher Scientific, you will do ambitious work, and be part of a team that values performance, quality, and innovation. As a member of a successful, growing global organization, you will be encouraged to perform at your best. With revenues of $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world. As part of our global team, what you do contributes directly to our Mission:- enabling our customers to make the world healthier, cleaner and safer, alongside receiving strong support for your own career growth . Fisher Clinical Services, part of Thermo Fisher Scientific, has an unwavering commitment to service, science and process engineering, Fisher Clinical Services is powered by people with an exceptional commitment to quality, deeply instilled ethics of personal responsibility and unrivalled expertise. We are exclusively focused on serving the packaging and distribution requirements of clinical trials across the world. Whether planning, packaging, labelling, storing, or distributing the important supplies needed to perform clinical research, for more than 27 years Fisher Clinical Services has been committed to delivering the highest possible value while ensuring adherence to the highest level of quality, performance, reliability and sustainability standards. How will you make an impact? Position Summary & Key Responsibilities : We’re looking for a dynamic, detail orientated individual, to assist the Quality Assurance (QA) team to complete required reviews to ensure products are packaged to high quality standards. You’ll do this by executing daily pre-approval, post-production and supporting documentation reviews to required standards and business needs within one of the QA disciplines (Clinical or Commercial). QA Responsibilities · Pre-approval of Clinical or Commercial packaging orders and associated documents · Post-production review of Clinical or Commercial batch records · Execute Quality review of Clinical or Commercial supporting documentation · Archive – assist with archiving of Clinical or Commercial batch records · Perform other relevant additional duties as requested by the QA Supervisor Experience, Knowledge & Skills: · Understanding of GxP pharmaceutical packaging/distribution activities · Skilled in degree of accuracy, concentration, verbal and written communication · Ability to cooperate with inter department team to provide support to other colleagues · Ability to prioritise own workload to deliver personal and team objectives within set timeframes · A-level or equivalent in relevant subjects or equivalent experience required How will you get here? · Demonstrate behaviours in line with the Thermo Fisher Core Competencies and 4i Values. · Takes ownership, accepts responsibility for your actions and always make sound decisions with solid communication skills. · Demonstrate an adaptive and flexible work style shown to be effective working across varied types of clients, product types and front-line team members. · Ensure compliance with cGMP and training requirements are met in line with business need. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us . As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. REQUIREMENTS: • Minimum 2 years experience in document control or quality systems in a regulated environment • Preferred Fields of Study: science, business administration, or related field • Relevant technical certifications in GMP/GxP documentation practices a plus • Proficiency in document management systems and quality control software (e.g., Agile, SAP, OCPLM, TrackWise) • Strong working knowledge of GMP requirements and documentation practices • Advanced Microsoft Office skills, particularly in Excel and Word • Excellent attention to detail and organizational abilities • Strong written and verbal communication skills • Ability to manage multiple priorities and meet deadlines • Experience with change control procedures and quality management systems • Additional language skills beneficial • Demonstrated ability to work independently and collaborate effectively with cross-functional teams • Experience with batch record review and documentation preferred • Knowledge of regulatory requirements in pharmaceutical/medical device industry
HQI 75
At AKQA we believe in the imaginative application of art and science to create beautiful ideas, products and services. With an entrepreneurial and collaborative approach, we design adaptive digital services and applications that capture the imagination, delivering impressive returns for our clients. You will love working in a team of highly skilled people, all with strong opinions about various technologies, frameworks and approaches to delivery. You will be able to articulate your ideas to your colleagues effectively and will take on board the ideas of others. You will thrive when faced with new challenges and will constantly look to improve clients’ deliverables. As a Senior QA Engineer, you are responsible for ensuring that all projects are delivered to specification and quality goals by leveraging tools, frameworks and programmatic techniques. An ideal candidate for this role matches the following role requirements and carries the below qualities & characteristics. ROLE REQUIREMENTS 6+ years of experience in QA with at least 3+ years in applying tools, frameworks and programmatic techniques to quality assurance of web, mobile web, and mobile apps. Expertise in executing manual test cases and scripts for products under development using test management/ tracking tools. Strong experience in implementing QA automation using code-based frameworks such as Cypress / Playwright. Strong experience with codeless automation tools such as Ghost Inspector. Experience testing web services / APIs using API automation testing tools such as Postman. Experience testing emails using Litmus / Email On Acid. Experience in one or more NFR testing areas such as Security, Load and Performance using tools like JMeter, Load Runner and OWASP. Experience in integrating QA automation / NFR scripts with DevOps tools such as Jenkins / Teamcity. Experience using CMS systems such as AEM & Contentful as part of the technology solution - either in a Traditional or Headless implementation. Experience using QA Cloud / SaaS platforms such as Applitools / Saucelabs / BrowserStack Experience in estimating, planning and coordinating testing activities for small to medium complexity projects. Experience in creating detailed test plans and test cases based on functional and non-functional requirements. Exposure to web accessibility testing and client-side performance testing. QUALITIES AND CHARACTERISTICS Versatile and able to adapt to frequently changing schedules and priorities in a fast-paced, agile environment. Strong oral and written communication; able to communicate effectively within a company’s diverse culture. Ability to make decisions and assertiveness. Proactive learner with a diverse interest across different QA tools & techniques. Passionate about Quality Teamwork We believe great work happens when we're together, fostering creativity, collaboration, and connection. That's why we’ve adopted a hybrid approach including required in-office days. If you require accommodations or flexibility, please discuss this with the hiring team during the interview process. AKQA is an equal opportunity employer and considers applicants for all positions without discrimination or regard to particular characteristics. We are committed to fostering a culture of respect in which everyone feels they belong and has the same opportunities to progress in their careers. About WPP WPP is the trusted growth partner for the world’s leading brands. We unite cutting-edge media intelligence and data solutions, world-class creativity, next-generation production, transformative enterprise solutions and expert strategic counsel in a single company – powered by exceptional talent and our agentic marketing platform, WPP Open, to help our clients navigate change, capture opportunity and deliver transformational growth. For more information, visit WPP.com.
HQI 90
Nium, the Leader in Real-Time Global Payments Nium, the leading global infrastructure for real-time cross-border payments, was founded on the mission to deliver the global payments infrastructure of tomorrow, today. With the onset of the global economy, its payments infrastructure is shaping how banks, fintechs, and businesses everywhere collect, convert, and disburse funds instantly across borders. Its payout network supports 100 currencies and spans 190+ countries, 100 of which in real-time. Funds can be disbursed to accounts, wallets, and cards and collected locally in 40 markets. Nium's growing card issuance business is already available in 34 countries. Nium holds regulatory licenses and authorizations in more than 40 countries, enabling seamless onboarding, rapid integration, and compliance – independent of geography. The company is co-headquartered in San Francisco and Singapore. About the role: The Quality Assurance Analyst is a member of the Regulatory Compliance Team, responsible for systematically verifying the accuracy, reliability, and compliance of financial operations and internal controls. Key Responsibilities: • Operational effectiveness testing – reviewing the timeliness, completeness and accuracy of Financial Crime Compliance Controls • Design effectiveness testing – review Standard Operating Procedures and assess against policy requirements • Planning – Complete Terms of Reference templates and deduce samples using approved sampling methodology for QA reviews • Reporting – present observations to senior stakeholders for factual accuracy discussions • Issue management – ensure all issues are remediated in a timely manner • Record-Keeping & Audit Readiness - ensure that thorough documentation of QA processes and results is maintained. Verify that all compliance documentation, records of AML/CFT activities, decisions, and reports, are properly kept and readily accessible for internal or external review and audits. Requirements : • Minimum 3+ years of financial crime, Compliance, Audit or QA experience • Experience with transaction monitoring, sanctions screening, KYC/EDD, and suspicious activity reporting. • Excellent stakeholder management and regulatory engagement experience. • Strong analytical, decision-making, and problem-solving skills. • Excellent written and verbal communication skills. • Experience using Artificial Intelligence (AI) to automate manual processes in a controlled environment. • Familiarity with AML transaction monitoring, CDD and Screening systems and e xperience managing regulatory examinations and remediation programmes.
HQI 93
S'more about the team We are looking for a Food Safety & Quality Assurance Supervisor who will take a hands-on approach to the maintenance and continuous improvement of our food safety management system. Reporting to the FSQA Manager, you will supervise a high-functioning team of FSQA Technicians, providing them guidance and acting as a key decision maker when food safety issues arise.. As part of the Food Safety & Quality Assurance team, you will play a key role in ensuring our customers receive high quality and safe meal kits they feel excited about serving to their families. Lettuce share what this role will be responsible for: Assign and monitor food safety related programs, including but not limited to pre-op inspections, environmental monitoring, pest control and GMP monitoring. Perform trend analysis on monitoring data; utilize results to drive improvements and close gaps. Conduct root cause analysis and implement corrective action plans for product and process non-conformances. Work closely with the Quality & Technical Team on product and packaging testing. Provide support for HACCP reassessment and new process development activities. Manage FSQA-related on-boarding, ad hoc and annual re-training. Assist with internal, CFIA and third-party audits and inspection. Act as primary escalation point and back-up to FSQA Manager in their absence. Manage team scheduling, attend team meetings, assist in complaint investigations and other tasks as assigned by the FSQA Manager. Work in compliance with OH&S acts and regulations. Use personal protective and safety equipment and clothing as directed by the employer and report workplace hazards and dangers to the supervisor or employer. Other duties as assigned Sound a-peeling? Here's what we're looking for: 3+ years in a food safety or quality assurance role in the food or other regulated industry. 1+ years of supervisory experience is considered an asset. Post-secondary education in Biological, Chemical or Food Sciences or equivalent experience. Understanding of HACCP principles, the Safe Food for Canadians Regulations and GFSI schemes. Strong leadership and communication skills. Excellent organizational and time management skills. Familiar with MS Office, Google Apps and comfortable learning and using new technology. Comfortable working in a deadline-driven and fast-paced environment. Flexible with working hours for business requirements, including early morning and late-night shifts. Let’s cut to the cheese, this is why you'll love it here: Box Discount - Amazing discounts on 1 box per week! 75% discount on weekly HelloFresh and Chefs Plate meal kits AND 50% off weekly Factor meal box. Health & Wellness - Health & Dental benefits from day 1, a Health Spending Account, unlimited access to the Headspace app to meet your self-care needs, and 25% discount on GoodLife fitness memberships! RRSP Matching - Competitive RRSP matching program offered Vacation & PTO - Time off is also an important part of self-care! We offer generous vacation and PTO to help you create a good work-life balance. Family Benefits - A parental leave top-up program for expectant parents. Growth & Development - We support your career progression, provide development opportunities, and invest in your continued learning through our organization wide L&D fund. Work Hard & Have Fun - From team socials to engaging company days, you’ll have plenty of opportunity to experience the fun! Diversity & Inclusion Initiatives - With impactful ERG’s like FreshPride, Women Empowered and LIMES, we are committed to our diversity, equity & inclusion efforts. Food Puns - this one is kind of a big dill if you haven’t already noticed. We even have some punny meeting room names! Working Conditions: It’s no surprise that as a food company, we use many ingredients that may be considered common allergens (i.e. peanuts, tree nuts, milk, etc.). Whether this role is based out of our headquarters or one of our distribution centers, it is possible that you may be exposed to such allergens in this role. If you have any concerns with being exposed to any particular food ingredients, including meat, please disclose this during the hiring process. If this sounds like you, please click the "Apply Now" button. If this role doesn't quite match what you're looking for, but you'd like to know more about joining the HelloFresh team, please visit our Jobs page to view our other vacancies. We'd love to hear from you! HelloFresh Canada uses AI-integrated technology to help us process and evaluate applications more efficiently. This includes tools that screen and assess candidate qualifications based on the requirements for this role. While these tools assist our workflow, all final selection decisions are made by our hiring team. This is a posting for an existing vacancy. We are actively seeking to fill this position. #factor #JD1008 Mississauga, ON Pay Range $63,000 — $73,000 CAD
HQI 86
Job Profile Description Provides independent, visible Quality Assurance leadership at the source of cell therapy manufacturing. This is a shift-based role scheduled for four days per week, Wednesday through Saturday. Partners with Manufacturing and supporting functions to apply risk-based quality judgment, resolve issues within established frameworks, and support reliable, compliant execution. Operates independently across qualified routine and moderately complex situations, influences cross-functional decisions, and strengthens quality culture through practical coaching, clear communication, and disciplined follow-through. Specific quality-system responsibilities and approval authorities are defined through applicable procedures, qualifications, and delegated authority. This is a shift-based role scheduled four days per week, Wednesday through Saturday . Typical Accountabilities • Maintain a consistent Quality presence in manufacturing areas and provide real-time, practical guidance that supports safe, compliant, and reliable execution. • Support manufacturing unit operations from a Quality Assurance perspective and assist to resolve manufacturing events and/or quality events in real-time • Independently assess routine and moderately complex quality situations, integrate available facts and risk considerations, and determine appropriate action or escalation within established standards. • Partner across functions to clarify requirements, align decisions, remove barriers, and sustain appropriate Quality independence. • Recognize emerging risks, recurring issues, and performance gaps; communicate implications and recommend proportionate actions. • Lead defined problem-solving and improvement activities, ensuring decisions are evidence-based, clearly documented, and carried through to effective resolution. • Coach colleagues on quality thinking, disciplined execution, data integrity, contamination control, and right-first-time behaviors. • Contribute quality judgment to operational meetings, shift handoffs, readiness discussions, and cross-functional decision forums. • Manage multiple priorities independently, communicate changes in risk or urgency, and maintain reliable follow-through in a fast-paced patient-focused environment. • Support inspection readiness and represent Quality confidently within the scope of training, experience, and delegated authority. • Work a shift-based schedule of four days per week, Wednesday through Saturday, and support occasional off-hours or holidays as needed for manufacturing operations and patient commitments. • The role may require additional responsibilities as necessary. Qualifications and Skills QA ATS Specialist Required Education and Experience: • 5+ years applicable quality experience with B.S. degree in Science, Engineering or related technical field • 9+ years applicable with Associates degree • 13+ years applicable with High School Diploma • Proven ability to work in a fast-paced environment across multiple technical functions • Strong knowledge of cGMPs • Demonstrated ability to make decisions under pressure that balance patient safety, compliance and supply Preferred Experience: • Autologous cell therapy manufacturing or quality experience • Working knowledge of international Cell Therapy GxP regulatory frameworks, regulations and guidance The annual base pay for this position ranges from $79,890 - $119,835. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans . Date Posted 21-Oct-2026 Closing Date 03-Nov-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
HQI 86
Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description The Quality Assurance team is responsible for reviewing and supporting equipment validations, process validations, change control, technical transfers, quality planning, gap assessments, and internal and external audit activities. Validation responsibilities include performing risk assessments to determine the appropriate extent of validation required. The QA Specialist II is responsible for writing and/or reviewing validation protocols and reports and supporting documentation associated with validation and change control processes. The application of risk assessment methodologies is required to support a fast-paced Change Control system while maintaining applicable IVD regulatory, quality system, and compliance requirements. Responsibilities include evaluating proposed changes for quality and regulatory impact, identifying potential risks and gaps, and ensuring appropriate controls and documentation are established. Quality planning responsibilities include supporting the development, implementation, and maintenance of quality plans for new and existing products, processes, projects, and quality system initiatives. The QA Specialist II collaborates with cross-functional teams to define quality requirements, deliverables, acceptance criteria, risk controls, and quality activities throughout the applicable product and process lifecycle. This position also monitors quality plan activities and deliverables to ensure requirements and commitments are completed in accordance with established timelines. Gap assessment responsibilities include conducting and/or supporting assessments of processes, procedures, documentation, and quality system elements against applicable internal requirements, standards, regulations, and business requirements. The QA Specialist II identifies and documents gaps, evaluates associated quality and compliance risks, recommends appropriate remediation activities, and partners with process owners and cross-functional teams to develop and track action plans through completion. Gap assessments may be performed in support of new or revised requirements, quality system improvements, inspection readiness, site or process changes, and other compliance initiatives. Technical Transfer activities include reviewing protocols and reports and collaborating cross-functionally to develop robust manufacturing processes, QC methods, specifications, and documentation supporting the Device Master Record (DMR). The QA Specialist II provides Quality oversight throughout transfer activities to help ensure applicable quality and regulatory requirements are appropriately incorporated and documented. Audit responsibilities include supporting and participating in internal audits, external audits, and regulatory inspections, as applicable. The QA Specialist II may assist with audit preparation and readiness activities, review documentation for compliance with established procedures and applicable regulatory requirements, gather and present objective evidence, respond to auditor requests, and support the documentation, investigation, and timely closure of audit observations and findings. Responsibilities may also include supporting corrective and preventive actions (CAPAs) resulting from audits, tracking commitments through completion, and collaborating with cross-functional teams to maintain a state of inspection readiness and drive continuous improvement. The QA Specialist II may serve on Core Teams or assist Core Teams in developing processes and transferring knowledge across functional groups. This position is highly cross-functional and requires independent judgment, effective communication, attention to detail, risk-based decision-making, and adherence to established schedules and commitments while working under moderate levels of guidance. Location: West Hills, CA. Relocation assistance is NOT provided. • Must be legally authorized to work in the United States without sponsorship. • Must be able to pass a comprehensive background check, which includes a drug screening. Key Responsibilities • Review validation projects, protocols, and reports in support of equipment and process validation. view PDF filesexternally in Adobe Acrobat. • Write and review protocols and reports. • Review IQ/OQ protocols and reports. • Assist in Risk Assessment exercises in support of validation activities. • Collaborate with R&D, Product Development Manager, Technical Operations, and Operations to ensure successful process development and technical transfers. • Coordinate validation activities/reviews in support of assigned validation projects working closely Subject Matter Experts. • Recommend approval or failure of validation studies. • Maintain knowledge and comprehensive understanding of relevant Medical Device regulations and current interpretations affecting equipment, product and process validation. • Act as a resource to other departments for product and process knowledge. • Able to work independently, with guidance from the Quality Assurance team. • Ability to learn new products and technology. • Able to successfully lead a project involving a peer group. • Lead and/or participate in product related team meetings and/or performance reviews, as needed. • Assist with QA department functions as needed. (Specific duties may vary and will be documented in department records, job assignments and/or project action items). • Perform computer operations for data entry and provide tracing/trending reports. • Additional support of routine QA department standard operating procedures (SOPs) is also expected when necessary. • Exhibits a high level of quality (right the first time), integrity (do what you say you are going to do), and cross functional behavior (always stay above the line). • Embody the Thermo Fisher 4-I Values at all times Minimum Requirements • Bachelor’s degree in Biology, Chemistry, or other similar Life Science field. • 3+ years relevant experience in Quality regulated environment • Detailed knowledge of ISO and GMP regulations which govern a medical device and diagnostics manufacturing • Able to create presentations, work with spreadsheets, prepare reports and write procedures utilizing MS Word, Excel and PowerPoint software applications. • Consistently demonstrated validation proficiency, with knowledge of equipment qualification (IQ/OQ/PQ), process validation, and computer/automation systems. • Good analytical skills, with an ability to use scientific knowledge and statistical methods to identify root causes of process and product failures. • Strong project management and organizational skills. • Demonstrated technical skills in process validation & concepts with an emphasis on implementation. • Excellent verbal and written communication skills. • Previous experience in problem solving methodology. • Possess a continuous process improvement mindset with the ability to effectively lead and manage change. • Performs all job duties in a safe manner, consistent with the Code of Ethics and the Thermo Fisher Scientific 4-I core values of Integrity, Intensity, Innovation, and Involvement. • Performs other duties as assigned. Compensation and Benefits The salary range estimated for this position based in California is $67,400.00–$101,150.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: • A choice of national medical and dental plans, and a national vision plan, including health incentive programs • Employee assistance and family support programs, including commuter benefits and tuition reimbursement • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
HQI 83
Reference no. R2871503 Position title: Quality Assurance Specialist Department: QA DS B89/90 Location: Toronto, ON About the job Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. Our Team/ Overview: The Quality Assurance team serves as a critical guardian of patient safety and product excellence through rigorous GMP record review and batch release activities, while fostering a culture of quality ownership and continuous improvement across operations. Through systematic oversight and shopfloor expertise, we proactively identify and mitigate quality risks, maintain robust quality systems, and ensure full regulatory compliance. Our collaborative partnerships across all functions embed quality principles into every aspect of operations, enabling the timely delivery of high-quality products to patients while upholding the highest standards of operational excellence. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main responsibilities: • Ensuring that activities in his/her scope are conducted in compliance with applicable regulatory requirements • Ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations • Conducting regular audits of production processes to identify and address potential quality issues • Collaborating closely with production to ensure quality standards are maintained throughout the product lifecycle; highly recommended to be located on the shopfloor • Managing and resolving quality-related issues in a timely and effective manner • Monitoring and analyzing quality performance metrics, implementing corrective actions as needed • Leading root cause analysis investigations for quality incidents and implementing preventive measures • Participating in internal and external audits and regulatory inspections providing support and documentation • Developing and implementing risk management strategies to mitigate potential quality issues • Fostering a culture of quality and continuous improvement across the organization Section 3: Key Involvement in Decision-Making Process Key Roles (D,A,I) • Request corrections when GMP rules are not respected (D) • Prioritize quality and compliance objectives (A) • Proactively implement remediation action from findings from internal and external audits related to quality issues (D) • Request quality improvement initiatives and strategies (D) • Identify discrepancies and corrective/preventive actions that need to be taken (D) • Escalate to upper management any failure in GMP execution on shopfloor (I) • Inform relevant stakeholders and team members of quality performance, corrective actions, findings, and preventive measures (I) • Advise on how to present a topic and answer specific questions (A) • Advise on risk management strategies and plans (A) • Advise on initiatives to promote a quality-focused culture (A) Section 4: Local specificities Additional Accountabilities • Provide QA support to any required APU or PCU on site as designated by the QA Ops Manager & PCU Lead • Any other duties that may arise as required About you Education / Experience Requirements: • Bachelor's degree or higher preferably in Pharmacy, Chemistry, Biochemistry, Life Sciences, Chemical Engineering, or a related scientific field • Minimum 2 years of experience in pharmaceutical quality assurance or operations (depending on level) Technical Skills: • Demonstrated experience in Drug Substance / Drug Product (DP) quality operations • Working knowledge of cGMP and GxP regulations in a regulated pharmaceutical environment • Experience with quality documentation, compliance activities, and regulatory requirements • Familiarity with change control processes and quality systems • Background in process improvement and quality investigations • Quality Assurance and Change Control Processes • Inspection Readiness • Root Cause Analysis / RCA / Preventive Action • Regulatory Requirements • QA Standards • Documentation Review • Manufacturing Processes • Product Quality Assurance • Risk Management • Cross-Team Communication and Collaboration • Stakeholder Management Why Choose Us? • Bring the miracles of science to life alongside a supportive, future-focused team. • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs. This position is for a new vacant role that is now open for applications. AI Usage "Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal, Data Subject Rights Webform . The Data Subject Rights Webform can also be used to request access or correction of your personal information and file a complaint. Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request #GD-SP #LI-SP #LI-Onsite Pursue progress , discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com ! North America Applicants Only The salary range for this position is: 76,200.00 - 110,100.00 Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefits programs, and additional benefits information can be found through the (CA) LINK OR (US) LINK . La fourchette salariale pour ce poste est la suivante: 76,200.00 - 110,100.00 La rémunération finale sera déterminée en fonction de l'expérience démontrée, des compétences, du lieu de travail et d'autres facteurs pertinents. Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise, et des informations supplémentaires sur les avantages sociaux peuvent être trouvées via le lien
HQI 91
S'more about the team We are looking for a Food Safety & Quality Assurance Supervisor who will take a hands-on approach to the maintenance and continuous improvement of our food safety management system. Reporting to the FSQA Manager, you will supervise a high-functioning team of FSQA Technicians, providing them guidance and acting as a key decision maker when food safety issues arise.. As part of the Food Safety & Quality Assurance team, you will play a key role in ensuring our customers receive high quality and safe meal kits they feel excited about serving to their families. Lettuce share what this role will be responsible for: Assign and monitor food safety related programs, including but not limited to pre-op inspections, environmental monitoring, pest control and GMP monitoring. Perform trend analysis on monitoring data; utilize results to drive improvements and close gaps. Conduct root cause analysis and implement corrective action plans for product and process non-conformances. Work closely with the Quality & Technical Team on product and packaging testing. Provide support for HACCP reassessment and new process development activities. Manage FSQA-related on-boarding, ad hoc and annual re-training. Assist with internal, CFIA and third-party audits and inspection. Act as primary escalation point and back-up to FSQA Manager in their absence. Manage team scheduling, attend team meetings, assist in complaint investigations and other tasks as assigned by the FSQA Manager. Work in compliance with OH&S acts and regulations. Use personal protective and safety equipment and clothing as directed by the employer and report workplace hazards and dangers to the supervisor or employer. Other duties as assigned Sound a-peeling? Here's what we're looking for: 3+ years in a food safety or quality assurance role in the food or other regulated industry. 1+ years of supervisory experience is considered an asset. Post-secondary education in Biological, Chemical or Food Sciences or equivalent experience. Understanding of HACCP principles, the Safe Food for Canadians Regulations and GFSI schemes. Strong leadership and communication skills. Excellent organizational and time management skills. Familiar with MS Office, Google Apps and comfortable learning and using new technology. Comfortable working in a deadline-driven and fast-paced environment. Flexible with working hours for business requirements, including early morning and late-night shifts. Let’s cut to the cheese, this is why you'll love it here: Box Discount - Amazing discounts on 1 box per week! 75% discount on weekly HelloFresh and Chefs Plate meal kits AND 50% off weekly Factor meal box. Health & Wellness - Health & Dental benefits from day 1, a Health Spending Account, unlimited access to the Headspace app to meet your self-care needs, and 25% discount on GoodLife fitness memberships! RRSP Matching - Competitive RRSP matching program offered Vacation & PTO - Time off is also an important part of self-care! We offer generous vacation and PTO to help you create a good work-life balance. Family Benefits - A parental leave top-up program for expectant parents. Growth & Development - We support your career progression, provide development opportunities, and invest in your continued learning through our organization wide L&D fund. Work Hard & Have Fun - From team socials to engaging company days, you’ll have plenty of opportunity to experience the fun! Diversity & Inclusion Initiatives - With impactful ERG’s like FreshPride, Women Empowered and LIMES, we are committed to our diversity, equity & inclusion efforts. Food Puns - this one is kind of a big dill if you haven’t already noticed. We even have some punny meeting room names! Working Conditions: It’s no surprise that as a food company, we use many ingredients that may be considered common allergens (i.e. peanuts, tree nuts, milk, etc.). Whether this role is based out of our headquarters or one of our distribution centers, it is possible that you may be exposed to such allergens in this role. If you have any concerns with being exposed to any particular food ingredients, including meat, please disclose this during the hiring process. If this sounds like you, please click the "Apply Now" button. If this role doesn't quite match what you're looking for, but you'd like to know more about joining the HelloFresh team, please visit our Jobs page to view our other vacancies. We'd love to hear from you! HelloFresh Canada uses AI-integrated technology to help us process and evaluate applications more efficiently. This includes tools that screen and assess candidate qualifications based on the requirements for this role. While these tools assist our workflow, all final selection decisions are made by our hiring team. This is a posting for an existing vacancy. We are actively seeking to fill this position. #factor #JD1008 Mississauga, ON Pay Range $63,000 — $73,000 CAD
HQI 79
At Riot, we believe Quality is a set of values, practices, and behaviors that inform every part of the development process. By honing our craft of quality and demonstrating cross-discipline partnerships we help Riot sustainably craft excellent experiences for players, globally. As a Manager of Quality Assurance on VALORANT , you will lead quality strategy and people across some of VALORANT’s most technically complex and cross-cutting domains. You will manage quality owners responsible for a variety of areas within the game and your primary focus will be on the Game Engine, Technical Art, and Release Engineering that power VALORANT. You will be accountable for defining and executing a comprehensive test strategy that supports multiple cross-functional development teams, while shaping and promoting the vision of quality assurance across Riot—so that, “Gamers worldwide know that every experience they have with Riot will be a quality experience.” You will also ensure the execution of all test coverage within your product space, including playtest activities, manage testing, telemetry, defect data and report regularly on product quality. You will mentor your reports on the testing activities needed to support production within the teams you support. You will report into Riot Sydney Studio Leadership for VALORANT. Responsibilities: • Lead and manage QA professionals working across multiple teams and areas of VALORANT, with a specific focus on Foundations. • Hold teams accountable for upholding quality and player impact as an essential factor in decision-making • Partner with other craft leaders to influence craft and product decisions through quality insights and risk analysis • Assesses quality, risk, and complexity, and communicates clear mitigations and priorities to development teams and leadership • Coaches and supports direct reports through complex quality challenges, representing their plans and needs with initiative leadership • Partners with other disciplines to improve development workflows and define quality bars or targets that align with initiative goals • Monitors quality health and defect trends, maintaining data-driven reporting and continuous improvement systems that inform decision-making • Drives quality feature planning and executes testing coverage plans with teams Required Qualifications: • 5+ years Quality Assurance Experience, with experience in a leadership role • Performance test tooling and automation • Experience creating test strategies for products • Experience with test design, planning and control • Experience with product development pipelines and workflows • Experience managing performance of embedded QA professionals • Experience working with remote testing teams • Experience establishing quality metrics that influence strategy and drive change Desired Qualifications: • Experience in agile work systems • Experience delivering GaaS on any platform • ISTQB Foundation Level • ISTQB Agile Tester or ICAgile Agile Testing (ICP-TST) • ISTQB Expert Level • ISTQB Advanced Test Manager • Experience with Game Engine quality • Experience with software release and deployment pipeline quality • Experience testing on the Playstation 5 or Xbox Series S/X For this role, you'll find success through craft expertise, a collaborative spirit, and decision-making that prioritizes the delight of players. We will be looking at your past studies, experience, and your personal relationship with games. If you embody player empathy and care about players' experiences, this could be your role! Our Perks: At Riot we strongly believe in work / life balance, and we encourage that with our open paid time off policy, paid parental leave (for both primary and secondary carers) and flexible work schedules to fit your lifestyle. We also believe that work should be fun, we have co-op gaming areas, a play fund so you can broaden and deepen your knowledge of players and community, and all the snacks you would ever need to power through your day (even healthy snacks!). And that’s not all we offer, there’s also: • Medical Insurance that covers you and your dependents • Employee Assistance Program • Wellness fund • Donation matching of time and money to registered charities • Learning and Development opportunities At Riot Games, we put players first . That mission drives every decision in our quest to create games and experiences that make it better to be a player. Whether you’re working directly on a new player-facing experience or you’re supporting the company as a whole, everyone at Riot is part of our mission. And just like in our games, we’re better when we work together. Our goal is to create collaborative teams where you are empowered to bring your unique perspective everyday. If that sounds like the kind of place you want to work, we’re looking forward to your application.
HQI 86
At AstraZeneca's Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying , and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our fervor for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. Position Summary The Specialist, Quality ensures compliance with quality system's procedures and assessing regulatory and quality risks in activities and processes according to regulatory agency guidelines and company practices. This unique role is accountable for routine Quality Assurance responsibilities related to the production and disposition of products manufactured and tested on behalf of Astrazeneca . This role is based in Tarzana , CA, and reports to the Manager, QA. Responsibilities • Provide quality assurance support across technical operations functions ( i.e. Manufacturing, Facilities & Engineering, Supply Chain, Quality Control, Analytical Development, Product Development/Manufacturing Sciences & Technology) within AstraZeneca to assure compliance to the quality manual and maintain collaborative quality relationships. • Lead deviations and laboratory investigations related to GMP manufacturing and analytical testing, respectively, with cross-functional owners. Determine corrective/preventative actions (CAPA) and Verification of Effectiveness ( VoE ) and drive timely implementation and closure. • Work with appropriate partners to manage change controls in a phase appropriate manner for clinical stage products that supports quality risk management ( i.e. New Product Introduction, New Facility, & Manufacturing Process Change Controls). • Provide ILT trainings for annual GMP/GDP, Quality Manual, Quality Risk Management, Deviation/CAPA, Change Control. • Work with QA doc control to ensure accurate issuance of batch record documentation ( i.e. lot/media batch records and in-process/QC/final product labels) to manufacturing. • Review routine manufacturing batch documentation and quality control data for in-process and finished product to support disposition and lot closure. • Perform approval of equipment alarm acknowledgements, equipment activation and PM/Calibration schedules in computerized asset and alarm management system(s). • Review routine material release documentation for quality release of raw materials used for manufacturing and quality control testing. Education and Experience • BA/BS i n biological sciences or a related field is required • 2-4 years GMP regulated industry experience. . • Proficient in cGMP regulations, quality systems and regulatory • Experience writing, evaluating and closing investigations, CAPAs and change control records. • Adapt best practices for stage appropriate products . When we put unexpected teams in the same room, we ignite ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Benefits • Short-term incentive bonus opportunity • Equity-based long-term incentive program • 401(k) plan \ • Paid vacation and holidays; paid leaves • Health benefits including medical, prescription drug, dental, and vision coverage. The annual base pay (or hourly rate of compensation) for this position ranges from $ 100,880.80 - $151,321.20 . Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans. Date Posted 20-Oct-2026 Closing Date 30-Oct-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
HQI 78
Placements24 is seeking an Automotive Quality Assurance Manager in Kimberley, Northern Cape. You will lead a QA team, ensure IATF 16949 compliance, and drive CAPA and continuous improvement across suppliers, R&D, production, and supply chain. The role requires a strong background in automotive quality management, leadership ability, and proficiency with quality tools and QMS software. A competitive package awaits in a collaborative Kimberley environment. J-18808-Ljbffr
HQI 78
Placements24 in South Africa seeks a highly skilled Remote Quality Assurance Manager for a technology firm serving the hospitality industry. This fully remote role leads a globally distributed QA team and defines testing strategies for web and mobile applications. You will oversee the QA lifecycle, implement automation, coordinate with development, product, and support, and drive quality metrics and best practices from home. J-18808-Ljbffr
📋
No applications yet
Browse jobs and start applying to see them here.
Updated just now
