What are the responsibilities and job description for the QA Doc Control Specialist position at R&D Partners?
Job Description
Job DescriptionCompany Description
Duties:
- Issuance of Patient and Non-Patient lot batch records, in-process and final product labels to Manufacturing according to ICTC Master Production schedule
- Issuance of logbooks, GMP protocols and other controlled documents upon request.
- Maintain master documents and records (both hardcopy and electronic) to ensure documentation is retrievable and files are accurate, complete, and well organized.
Qualifications:
- Bachelor’s degree in Life Sciences discipline preferred, not required.
- Required: solid Batch Record Release and Electronic Document Management System exp.
- Minimum of two (2) years QA document control experience in pharmaceutical or biopharmaceutical GMP based facility.
- Proficient with document change management and FDA quality systems
- Proficient in an eDMS system (specifically MasterControl)
R&D Partners is a national Life Science staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined Life Science staffing experience providing consulting, direct hire & outsourcing solutions to the Life Science industry.
Company Description
R&D Partners is a national Life Science staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined Life Science staffing experience providing consulting, direct hire & outsourcing solutions to the Life Science industry.
Location/Region: Philadelphia, PA
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