Eacademy Sanofi
Job Title:
QC Lab Team Supervisor
Location:
Swiftwater, PA
About the Job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The QC Lab Team Supervisor, Incoming Quality Material Release (IQMR) will operate under flexibility to perform the necessary activities to meet the business needs to ensure compliance requirements and manufacturing/release schedules are met. This position will have direct personnel management responsibilities.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities
Overseeing daily operations of the Incoming Quality Material Release (IQMR) department to ensure adherence to the committed scheduled plans
Maintaining his/her department in compliance with the GMPs and quality control processes defined according to internal and external quality requirements and regulations
Managing and training department staff, ensuring they follow best practices and safety guidelines
Ensuring his/her department staff is qualified to perform the testing execution by maintaining the department qualification matrix
Conducting routine GEMBAs to identify improvement opportunities
Ensuring accurate and timely testing of received samples according to his/her perimeter
Reviewing and approving department test results and reports
Maintaining department equipment by applying maintenance, qualification, and calibration plans to ensure accuracy and reliability of department activities
Investigating in a timely manner and resolving any quality events, issues, or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs
Lead internal projects and take action to ensure continuous improvement ideas are completed
Final release of incoming raw materials, incoming products and test reagents
cGMP Review of Control Logs and Raw Material Assay Reports
Raw Material and Finished Goods Batch Disposition
Establish and prioritize department objectives (A)
Contribute to develop and implement protocol (e.g., for validation, transfer, investigation) (A)
Elaborate training programs (D)
Advise on testing schedules and priorities (A)
Decide on the approval of test results (D)
Advise about equipment maintenance schedules (A)
About You Qualifications
Experience in quality within the pharmaceutical industry, including knowledge of current Good Manufacturing Practices (GMP) (US, Canada, Japan, Europe) and regulatory requirements
Ability to analyze complex data and test results to make informed decisions and identify areas for improvement
Strong leadership abilities to manage and motivate a team, ensuring high performance and adherence to quality standards
Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements
Proficiency in identifying issues and implementing effective solutions to resolve quality control problems
A minimum of 8–10 years of relevant experience in a cGMP controlled/pharmaceutical environment in lieu of a BA/BS in life sciences or a minimum of 3–5 years of relevant experience in a cGMP controlled/pharmaceutical industry with a BA/BS in life sciences
Excellent organizational, written, interpersonal, leadership and teamwork abilities
Experience in SAP, LabWare, Veeva, Microsoft 365 is preferred
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 and at least 14 weeks’ gender-neutral parental leave
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affinitive Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital status, domestic partnership or civil union status, sex, gender, gender identity or expression, sexual orientation, disability, veteran or military status or liability for military status, domestic violence victim status, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
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QC Lab Team Supervisor
Location:
Swiftwater, PA
About the Job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The QC Lab Team Supervisor, Incoming Quality Material Release (IQMR) will operate under flexibility to perform the necessary activities to meet the business needs to ensure compliance requirements and manufacturing/release schedules are met. This position will have direct personnel management responsibilities.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities
Overseeing daily operations of the Incoming Quality Material Release (IQMR) department to ensure adherence to the committed scheduled plans
Maintaining his/her department in compliance with the GMPs and quality control processes defined according to internal and external quality requirements and regulations
Managing and training department staff, ensuring they follow best practices and safety guidelines
Ensuring his/her department staff is qualified to perform the testing execution by maintaining the department qualification matrix
Conducting routine GEMBAs to identify improvement opportunities
Ensuring accurate and timely testing of received samples according to his/her perimeter
Reviewing and approving department test results and reports
Maintaining department equipment by applying maintenance, qualification, and calibration plans to ensure accuracy and reliability of department activities
Investigating in a timely manner and resolving any quality events, issues, or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs
Lead internal projects and take action to ensure continuous improvement ideas are completed
Final release of incoming raw materials, incoming products and test reagents
cGMP Review of Control Logs and Raw Material Assay Reports
Raw Material and Finished Goods Batch Disposition
Establish and prioritize department objectives (A)
Contribute to develop and implement protocol (e.g., for validation, transfer, investigation) (A)
Elaborate training programs (D)
Advise on testing schedules and priorities (A)
Decide on the approval of test results (D)
Advise about equipment maintenance schedules (A)
About You Qualifications
Experience in quality within the pharmaceutical industry, including knowledge of current Good Manufacturing Practices (GMP) (US, Canada, Japan, Europe) and regulatory requirements
Ability to analyze complex data and test results to make informed decisions and identify areas for improvement
Strong leadership abilities to manage and motivate a team, ensuring high performance and adherence to quality standards
Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements
Proficiency in identifying issues and implementing effective solutions to resolve quality control problems
A minimum of 8–10 years of relevant experience in a cGMP controlled/pharmaceutical environment in lieu of a BA/BS in life sciences or a minimum of 3–5 years of relevant experience in a cGMP controlled/pharmaceutical industry with a BA/BS in life sciences
Excellent organizational, written, interpersonal, leadership and teamwork abilities
Experience in SAP, LabWare, Veeva, Microsoft 365 is preferred
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 and at least 14 weeks’ gender-neutral parental leave
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affinitive Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital status, domestic partnership or civil union status, sex, gender, gender identity or expression, sexual orientation, disability, veteran or military status or liability for military status, domestic violence victim status, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
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