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Job Information
Insight Global Document Reviewer in De Soto, Kansas
Job Description
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 .
To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .
Skills and Requirements
Strong experience reviewing and reporting completed Batch Records
Proficient in Microsoft Office (Word, Excel, Teams),
Previous experience or knowledge of inventory control, tacking, and deviation management in a Document Management Software (Preferably SAP)
Strong organizational skills with a high attention to detail
Knowledge of Fermentation, compounding, serial production
Appetite to investigate and problem solve by identifying errors omissions, checking for open deviations, and ensuring batch records were executed properly - 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 null
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 employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to 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 oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HR@insightglobal.com.