Bioprocess Regulatory Medical Writer

PSG Global Solutions; Chesterfield (MO); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading global solutions provider in Missouri is seeking a talented technical writer to join their BRD organization within the Pharm Sci BTx team. The successful candidate will verify data in regulatory documents, assist with document tracking, and create drafts using existing templates. With a focus on detail-oriented work, this role requires at least 3-5 years of experience in technical writing and a scientific degree in fields such as Biology or Chemistry. Opportunities for training and career growth are provided.

Qualifications

• 3-5 years of experience in technical writing, preferably in regulatory documents.
• Experience in bioprocess or cell line development areas is desirable.

Responsibilities

• Assist with verification of data within regulatory documents or reports.
• Support bioprocess R&D teams in tracking document completion.
• Create drafts of new technical or regulatory documents.
• Assist authors in assembling, formatting, and proofreading content.

Skills

Excellent oral and written communications

Experience in technical writing of reports

Regulatory experience

Detail oriented

Education

BS or higher in Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar

Job description

A leading global solutions provider in Missouri is seeking a talented technical writer to join their BRD organization within the Pharm Sci BTx team. The successful candidate will verify data in regulatory documents, assist with document tracking, and create drafts using existing templates. With a focus on detail-oriented work, this role requires at least 3-5 years of experience in technical writing and a scientific degree in fields such as Biology or Chemistry. Opportunities for training and career growth are provided.