TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.
Job Description:
Must have some experience with document control in GMP environment
Identifies compliance/non-compliance with procedures and resolves necessary amendments to GMP documentation
Complete archiving and virtual archiving of documents (scanning, storing files, archiving hardcopy files) to ensure documents can be accessed for customer enquiries, audits and inspections
Running database queries and reports in addition to data entry
Prepares data for audits/inspections
Batch record format review
1-3 Years' Experience
Reviews documents for accuracy and sorts into designated storage areas.
HS Diploma or GED required
TekWissen® Group is an equal opportunity employer supporting workforce diversity.