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- Quality Assurance Engineering
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Company | MilliporeSigma |
Address | , Rocklin, 95677, Ca |
Employment type | FULL_TIME |
Salary | $49,500 - $148,900 a year |
Expires | 2023-06-28 |
Posted at | 1 year ago |
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
MilliporeSigma in Rocklin, CA is hiring a Quality Assurance Supervisor to ensure the compliance of the quality management system with standards and regulations for highly regulated IVD products. You are the supervisor of a small team of quality experts. With a strong understanding of quality, you organize the operational implementation of GMP processes and communicate intensively with production, laboratory and other specialist departments. You are involved in change and validation processes as well as deviations and complaints in order to identify general quality risks and work on them. You create quality documents and present them during audits and inspections. You support quality management reviews and report KPIs and quality metrics .
Who You Are:
Minimum Qualifications:
Our ranges incorporate all levels and career types available within this specific role, and are derived from relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
MilliporeSigma in Rocklin, CA is hiring a Quality Assurance Supervisor to ensure the compliance of the quality management system with standards and regulations for highly regulated IVD products. You are the supervisor of a small team of quality experts. With a strong understanding of quality, you organize the operational implementation of GMP processes and communicate intensively with production, laboratory and other specialist departments. You are involved in change and validation processes as well as deviations and complaints in order to identify general quality risks and work on them. You create quality documents and present them during audits and inspections. You support quality management reviews and report KPIs and quality metrics .
Who You Are:
Minimum Qualifications:
- 3+ years of experience working in a GMP environment
- Bachelor's degree in any Engineering or Life Sciences field
- 3+ years of experience working within Quality Assurance
- Strong understanding of FDA QSR, ISO 13485, EU IVD and EU IVDR standards and regulations
- Highly proficient in MS Office Software (Outlook, Teams, Word, Excel, PowerPoint)
- Excellent written, oral, and interpersonal communications skills
- Ability to apply knowledge of regulations and standards to Quality processes
- Knowledge of Audit, Complaint, Deviation/CAPA and Change Control procedures
- Basic knowledge with quality and business software applications Trackwise and SAP
- Ability to work in a team environment
- Strong analytical skills
- Project planning/project management skills
- Experience in management of trainings, risks, validations, data integrity and suppliers
Our ranges incorporate all levels and career types available within this specific role, and are derived from relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html
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