GMP Technical Writer
The businesses of Merck KGaA, Darmstadt, Germany St. Louis, Missouri, United States · $76K–$114K/yr
Pharmaceutical Manufacturing · 10,001+ employees
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About the role
The GMP Technical Writer is responsible for creating batch records for GMP manufacturing of custom biologic drug substances. This role collaborates with manufacturing, quality, and development teams to ensure robust documentation for tech transfer.
What they look for
Requirements
Candidates must hold a bachelor's degree in a life science discipline and possess at least 2 years of experience in GMP operations. Strong composition skills and technical knowledge of manufacturing equipment are required for this position.
Benefits
Full description
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 GMP Technical Writer at the St. Louis, MO site is responsible for the creation of batch records for use in GMP manufacturing of the new custom biologic drug substance. This role works functionally with Manufacturing, Process and Analytical Development, Quality, Project Management, and customers to develop robust manufacturing batch records for 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
Who You Are:
Minimum Qualifications:
- Bachelor’s degree in Biology, Chemistry, Biochemistry or other 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
- 3+ years writing technical documentation to support GMP operations
- 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
- Effective communication with internal departments and customers
RSREMD
Pay Range for this position: $75,700.00 - $113,500.00
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!
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