Senior Quality Assurance Specialist
2 weeks ago
Cytiva is at the forefront of providing innovative solutions to transform human health in the Life Sciences industry. Our customers undertake life-saving activities ranging from fundamental biological research to developing new medicines and cell therapies.
At Cytiva, you will work on challenges that truly matter with people who care for each other, our customers, and their patients. With associates across 40 countries, we offer a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term.
About the RoleThe Supplier Quality Engineer will collaborate with other functional areas and operating entities to effectively manage supplier quality requirements & supplier development. This role involves improving supplier quality performance for assigned suppliers via Quality Plan implementation, ensuring supplier compliance to Cytiva QMS and regulatory requirements through supplier monitoring process.
This position requires strong technical aptitude, with a strong background in interpretation of drawings / specifications, measurement method and manufacturing process planning / evaluation. The ideal candidate will have experience in supplier quality engineering, quality assurance, quality engineering, manufacturing, or engineering, preferably in the medical device, or pharmaceutical industry.
What You Will Do- Collaborate with other functional areas and operating entities to effectively manage supplier quality requirements & supplier development.
- Improve supplier quality performance for assigned suppliers via Quality Plan implementation.
- Ensure supplier compliance to Cytiva QMS and regulatory requirements through supplier monitoring process.
- Interface with suppliers and internal stakeholders to drive quality improvements that minimize the Costs of Quality and implement supplier/engineering changes, New Product Introductions and Transfers.
- Demonstrated ability to lead, develop, communicate & implement a strategy to ensure compliance to Cytiva, regulatory and industry requirements.
- Demonstrated technical aptitude: strong background in interpretation of drawings / specifications, measurement method and manufacturing process planning / evaluation.
- Proactive, self-driven, results seeking and enthusiastic intensity, with an eye for quality and compliance.
- Experience in supplier quality engineering, quality assurance, quality engineering, manufacturing, or engineering; preferably in the medical device, or pharmaceutical industry.
- Degree in an engineering or technical discipline or equivalent non-technical degree with experience in manufacturing, engineering or quality assurance.
- Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies and understanding of manufacturing processes.
- Knowledge of clean room production and sterility assurance.
- Desire and ability to travel up to 30% of the time.
We value diversity and the existence of similarities and differences found in our workforce, workplace and throughout the markets we serve.
Estimated salary range $85,000 - $115,000 per year, depending on location and experience.
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