QA Document Control Admin
Employment type: Contract
Location: Los Angeles Area
A growing Biotech/Pharma company is seeking to expand their QA department to help with some of the most important and relevant scientific projects of the decade.
Document Control Key Responsibilities
- dealing with GMP documentations and keeping a filing system in place
- Batch Records
- Verification/Scanning of documents
- Regulatory Audit prep
- improving the current Quality Systems
- Reporting into the QA team and maintaining processes across the job-site
Document Control Qualifications and Skills
- Degree in a science related field is helpful but not required
- Having worked in a previous GMP setting is a must
- Previous experience with a biotech/pharma organization
- Previous document control experience, at least 1 year
To find out more, please apply!