Production Document Reviewer

Job Description
Insight Global is seeking a first shift (7:00am-3:15pm) Documentation Specialist to support a pharmaceutical manufacturing operation by ensuring production documentation is completed accurately, thoroughly, and in compliance with cGMP and quality standards. This individual will be responsible for reviewing batch records, identifying documentation discrepancies, maintaining document control processes, and collaborating with cross-functional teams to support compliant manufacturing operations. The ideal candidate is detail-oriented, organized, and experienced working in a regulated GMP environment.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pre...