Technical Document Writer - Biomanufacturing

Collabera is looking for a Technical Document Writer - Biomanufacturing to write, review, and drive production and quality documentation to approval. The role will produce high-quality cGMP documentation contributing to project goals. Additional responsibilities include tracking daily, weekly, and monthly forecasted documentation priorities and collaborating with internal teams to generate and review new documents.

Requirements

• 3+ years of previous technical writing experience in a cGMP pharmaceutical environment
• Experience in manufacturing under cGMP guidelines and strong knowledge of cGMP requirements
• Prior experience working in a biotech/pharmaceutical company
• Exceptional written/verbal communication, listening, organizational, interpersonal, research, investigative, and problem-solving skills
• Proven ability to communicate complex ideas in a clear, concise manner
• Working knowledge of MS Office Suite and an Electronic Document Management System (EDMS)
• Experience with Document Proficiency in MS Office Products

Benefits

• Paid vacations
• Holidays
• Personal days
• Medical insurance
• Dental insurance
• Vision insurance
• 401K retirement savings plan
• Life Insurance
• Disability Insurance