St. Louis, Missouri, United States
21 hours ago
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 and existing custom bioconjugation products. This technically sound position works crossfunctionally 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 at our Cherokee site in St. Louis, Missouri.

 

Key Responsibilities:

Authorship of new product MMFs and associated technical documents Manage MMF priorities based on schedule and project requirements                                   Participate in process design flow efforts                                    Provide logical explanations and potential solutions for roadblocks to GMP                                Collaborate with other departments and external customers                                    Interface with management, other departments and customers to collaborate, identify, and implement tech transfer activities                                    Write and modify procedures consistent with quality guidelines and review other procedures as requested                                    Participate and assist deviation investigations from Technical Operations perspective  Identify and mitigate safety hazards with transferred manufacturing processes                                    

                     

Who You Are:
Minimum Qualifications:

Bachelor’s Degree in Biology, Chemistry, Biochemistry or other life science discipline1 + years’ experience in GMP Operations, manufacturing or production operations

 

Preferred Qualifications:

Excellent attention to detail in written instruction and communication Strong composition skillsAbility to convey technical, safety, and GMP compliance information and instruction through writingComprehensive technical knowledge and understanding of GMP manufacturing equipment and production processesAbility to effectively communicate with internal departments and customers


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

 

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