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Supervisor, Quality Control

 

A career with MilliporeSigma is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and electronics. 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.

 

Your role:

At MilliporeSigma, the Quality Control Supervisor will provide direct management and development of the department that is primarily responsible for testing and timely release of in-process, intermediate, final products.  Other areas of responsibility may include, raw materials, method validation / qualification, and stability testing associated with cGMP manufacturing.

 

  • Provide leadership and organize departmental staff to meet deadlines without compromising quality.
  • Demonstrate an understanding of analytical chemistry and laboratory procedures.
  • Ensure appropriate technical training is provided for QC personnel. 
  • Perform routine and non-routine tests. 
  • Operate analytical instrumentation, with working knowledge of spectral and chromatographic interpretation and troubleshooting.
  • Schedule and coordinate daily workload for laboratory analysts ensuring efficient use of resources with minimum product turnaround times.
  • Work in accordance with current GMPs and regulatory requirements.
  • Demonstrate proper laboratory safety and housekeeping practices.
  • Use department resources efficiently and works within departmental budget.
  • Identify areas for improvement and take action to undertake them through leadership and delegation to other members of the department.

  

 

Who You Are:

 

Basic Qualifications:

  • Bachelors Degree in Chemistry, Biology, Biochemistry, Chemical Engineering, or related life science discipline
  • 3+ years of quality experience in an active pharmaceutical ingredient, pharmaceutical, or related cGMP production environment
  • 2+ years management, supervisory, and or lead experience

 

Preferred Qualifications:

  • Ability to act in a position of leadership and work in analytical testing labs with hazardous/toxic chemicals.
  • Knowledge of Good Manufacturing Practices for pharmaceutical manufacturing (21 CFR 210 & 211) and/or Q7A Good Manufacturing Practice Guidance for API’s
  • Excellent organizational, written and verbal communication and interpersonal skills.
  • Knowledge and understanding of organic analytical chemistry

 

 

 

RSRMS

 

 

 

 

 

 

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.

Job Requisition ID:  217105
Location:  Madison
Career Level:  D - Professional (4-9 years)
Working time model:  full-time

Careers during Covid-19
Thank you for visiting our careers website, we are always looking for curious minds to join our teams. We understand how much the world is being impacted by the Covid-19 crisis and we want to assure you that your safety is very important to us. To ensure that everyone’s health is protected, instead of a standard face-to-face interview, it is likely that you will be offered alternative digital interview options.

US Disclosure
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.

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday.


Job Segment: Biochemistry, Manager, Housekeeping, QC, Science, Quality, Management, Healthcare

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