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Pharmaceutical Quality Assurance Specialist
- Contract
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a Pharmaceutical Quality Assurance Specialist for a top biopharmaceutical company located in Athens, GA.
Must be eligible to work or be a citizen in the US.
Job Responsibility:
- Facilitates timely and accurate archiving of GMP documentation
- Issues manufacturing harvest records, quality control assay worksheets, logbooks, etc.
- Reviews manufacturing harvest records to certify compliance with specifications and procedures.
- Supports and completes required documentation for batch disposition.
- Supports review of incoming materials for compliance to specifications, determines release status.
- Inputting information from the Quality Systems into electronic databases and generating reports from these systems.
- Capturing and reporting metrics around Quality Systems and Harvest Record review turn-around times and closure/approvals times.
- Collaborate with teams to ensure efficient, compliant, and timely review and closure of GMP documents
Skills and Requirements:
- Minimum of 0-2 years GMP related experience in biopharmaceutical / pharmaceutical or related industry experience
- High school degree required
- Bachelor's degree in Life Sciences Field preferred
- Familiar with cGMPs and regulatory requirements
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at (+1) 215-531-6914 or s.briggs@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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