GMP Technical Writer: Batch Records & Tech Transfer

MilliporeSigma; St. Louis (MO); On-site; USD 76,000 - 114,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement contributions

Perquisites

Job summary

MilliporeSigma in St. Louis, MO is seeking a GMP Technical Writer to create batch records for manufacturing a new biologic substance. You will partner with Manufacturing, Process and Analytical Development, Quality, and Project Management to produce robust Tech Transfer documents.

The ideal candidate has strong composition skills, detailed technical knowledge of GMP manufacturing equipment and processes, and excellent written communication to convey safety and compliance information.

Qualifications

• Bachelor’s degree in Biology, Chemistry, Biochemistry or Life Science discipline
• 2+ years’ experience in GMP Operations, manufacturing, or production operations
• Excellent attention to detail and strong composition and writing skills
• Ability to convey technical, safety and GMP compliance information through writing

Responsibilities

• Create batch records for GMP manufacturing of the new biologic drug substance
• Collaborate with Manufacturing, Process and Analytical Development, Quality, Project Management, and customers
• Develop robust Tech Transfer documents and batch records

Skills

Attention to detail

Composition skills

Written communication

Technical writing

Education

Bachelor’s degree in Life Science

Job description

MilliporeSigma in St. Louis, MO is seeking a GMP Technical Writer to create batch records for manufacturing a new biologic substance. You will partner with Manufacturing, Process and Analytical Development, Quality, and Project Management to produce robust Tech Transfer documents.

The ideal candidate has strong composition skills, detailed technical knowledge of GMP manufacturing equipment and processes, and excellent written communication to convey safety and compliance information.