What are the responsibilities and job description for the Document Reviewer position at Insight Global?
Insight Global is seeking a Document Specialist for a manufacturing site that will sit in De Soto, KS. This person will be primarily responsible for the review of executed (completes) batch records received from Manufacturing team. Review is to discover documentation errors, calculation errors, deviations from manufacturing instructions, or any other kind of exception. Processing / review of manufacturing batch documents will also require access to and actions within various systems for inventory control, tracking, and deviation management. Rate : 22 / hr-25 / hr
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 pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and / or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal. com.
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- Bachelors Degree or background in Bio Safety, Pharma, Technical Writing, Training, Quality Assurance, Quality Control, Life Sciences, or Validation
- Previous Pharma / manufacturing experience (Or Bio production, GMP)
Knowledge or previous experience with change management and deviation management from a quality perspective
Appetite to investigate and problem solve by identifying errors omissions, checking for open deviations, and ensuring batch records were executed properly
