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Supervisor, QC Chemistry - B Shift

 

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

 

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:

Supervise the QC analytical chemistry laboratory operations including product testing, data review and approval. In this role you are responsible for ensuring laboratory personnel adhere to standard operating procedures, business plans, and operates in a safe environment.


Responsibilities include but are not limited to: 

  • Supervising, training, and coaching of QC Laboratory staff.
  • Assuring operations in the lab are in compliance with cGMPs and Company SOPs/policies.
  • Overseeing the QC testing of finish product, raw materials, stability samples, engineering, and in-process materials.
  • QC laboratory’s Environmental, Health, and safety compliance.
  • Laboratory’s adherence to the business plan.
  • Reviews and approves of analytical test data.
  • Communicates QC operational issues to affected departments or as directed by QC’s Management.
  • Represent the QC Laboratory in a technical expert capacity on special studies and validations.
  • Lead non-conformance and OOS investigations within the laboratory.
  • B Shift: Monday - Friday 4pm - 12:30am. 


 

Who You Are:

Minimum Qualifications:

  • Bachelors Degree in Chemistry, Biology, or other Life Science Discipline. 
  • 5+ years of experience in a Quality Control role within the pharmaceutical industry.
  • 1+ years of experience with HPLC. 

 

Preferred Qualifications:

  • 2+ years of supervisory experience.
  • Strong leadership skills.
  • Strong communication skills.
  • Experience with QC systems operations.
  • Experience with GMP testing.
  • Experience working with a manufacturing environment.
  • Experience with chemistry analytical techniques.


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

 

Job Requisition ID:  285588
Location:  Indianapolis
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

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 Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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Nearest Major Market: Indianapolis

Job Segment: QC, Pharmaceutical, Laboratory, Environmental Health & Safety, Developer, Quality, Science, Healthcare, Technology

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