QC Manager, Life Sciences - Solon, OH, US

Only for registered members Solon, OH, US, United States

1 day ago

Default job background
About MP Biomedicals: · MP Biomedicals is a global life science company with headquarters in California and regional offices across the globe. The company offers a diverse portfolio of life science products, fine chemicals, and diagnostics used in industries ranging from basic r ...
Job description

About MP Biomedicals:
MP Biomedicals is a global life science company with headquarters in California and regional offices across the globe. The company offers a diverse portfolio of life science products, fine chemicals, and diagnostics used in industries ranging from basic research to clinical diagnostics and pharmaceuticals. Over the past 50 years, we have provided quality tools and expert services to assist our customers in making breakthrough discoveries and achieving scientific excellence.

Company Mission Statement:
Our mission is to empower global research that unlocks life-changing solutions and inspires a meaningful life.

Company Values:

  • Respect
  • Meaningful Work
  • Career Development
  • Accountability
  • Honesty

  • MP Biomedicals Benefits:

    • Bonus Pay
    • Monthly Childcare Credit
    • Free breakfast on Mondays
    • Free Catered Lunches Tuesday-Friday
    • Paid Vacation
    • Paid PTO Hours
    • 10 Paid Company Holidays per Year
    • 401k with Company Match
    • Competitive Healthcare Benefits
    • HSA
    • Company Paid Life Insurance and Short-term Disability
    • Learning and Development Program
    • Employee Referral Program
    • Employee Assistance Program
    • Employee Discounts
    • And so much more
    • The primary responsibilities of the QC Manager are:


      •  Lead and support QC laboratory staff through planning, coaching, mentoring, hands-on technical guidance, and troubleshooting, including the investigation and resolution of OOS and atypical test results.


      •  Develop, maintain, and improve laboratory procedures, test methods, and product specifications; support cost-saving initiatives and laboratory efficiency improvements.


      •  Plan, execute, and support instrument qualification and analytical method validation activities.


      •  Ensure all laboratory activities are conducted and documented in compliance with GLP requirements; review and approve final test results, data analyses, and spectral interpretations.


      •  Collaborate with QA on product investigations by designing and performing supplemental testing or experiments as needed.


      •  Ensure timely execution and documentation of laboratory preventive maintenance and instrument calibration.


      •  Serve as a primary point of contact for internal and external stakeholders, providing timely and accurate responses through established communication channels.


      •  Support laboratory inspections and audits (internal and external), maintaining continuous audit readiness through routine walkthroughs and compliance checks.


      •  Establish, monitor, and report key performance indicators (KPIs) to assess laboratory performance and drive continuous improvement.


      •  Provide ongoing mentorship and development support to direct reports, including performance management, career development, and succession planning.


      •  Participate in chemical spill response and cleanup activities in accordance with safety procedures.


      • The education requirements for the QC Manager are a Master's degree or Ph.D. in Biology, Microbiology, Immunology, Biochemistry, Chemistry, or similar field. 


      •  The QC Manager reports to the Director of Operations and has direct reports that include chemists and technicians. 




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