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A career with MilliporeSigma is an ongoing journey of discovery: our 51,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.
This Supervisor, Quality Control position will be for a weekend day shift. This is a 4 day shift with 10 hour days (approximate times with lunch break ~9:00am-7:30pm with flexibility) Friday, Saturday, Sunday, Monday and will include a shift premium stipend.
The primary responsibilities of the Supervisor, Quality Control position are to provide management of the Quality Control department which is responsible for method validation/qualification, testing and timely release of raw material, in-process, intermediate, final product, and stability samples associated with cGMP manufacturing. This position is responsible for supporting efforts to ensure the laboratory is compliant with regulatory requirements including oversight of the training program for QC personnel, maintenance and calibration of instrumentation, reference standard inventory program, and all supportive efforts undertaken in the testing of cGMP materials. Direct management, engagement, and development of Quality Control personnel are also primary responsibilities.
This position includes the oversight of analytical method transfers/qualification/validation into the QC laboratory, conducting analytical investigations, and testing using HPLC, GC, IC, GCMS, LCMSMS, KF, DSC, TGA, IR, NMR, Polarimetry, XRPD, UV-Vis, titration and other wet lab procedures. Experience with writing technical reports is required. Additional responsibilities may include oversight and participation in change control, instrument calibration including IQ/OQ/PQ/PM and troubleshooting, cleaning verification/validation program, stability program, environmental monitoring program, supplier qualification program, and other projects as assigned. Review of analytical results produced by analysis from cGMP testing is required. The Quality Control Supervisor position, like all positions at SAFC, will require a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.
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What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at https://jobs.vibrantm.com
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.