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GMP Technical Writer

 

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:

 

The Technical Writer is responsible for the creation of batch records for use in GMP manufacturing of new custom products. This technically sound position works cross functionally at multiple manufacturing facilities with Manufacturing, Process and Analytical Development, Quality, Project Management, and customers to develop robust manufacturing batch records from Tech Transfer documents. We’re looking for a candidate with strong composition skills and comprehensive technical knowledge and understanding of manufacturing equipment and production processes.

 

The position will be based in St. Louis, Missouri.

 

Who You Are

 

Minimum Qualifications:

 

  • Bachelor’s degree in Biology, Chemistry, Biochemistry or another life science discipline.
  • 2 + years’ experience in GMP Operations, manufacturing or production operations.

 

Preferred Qualifications:

 

  • 5 + years’ experience in GMP Operations, manufacturing or production operations.
  • 1+ years' experience writing GMP batch records.
  • Excellent attention to detail in written instruction and communication.
  • Strong composition skills – Able to convey technical, safety, and GMP compliance information and instruction through writing.
  • Comprehensive technical knowledge and understanding of GMP manufacturing equipment and production processes.
  • Ability to effectively communicate with internal departments and customers.

RSREMD


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:  277088
Location:  St. Louis
Career Level:  C - Professional (1-3 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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