We are seeking a highly motivated individual to join us as a Quality Systems Specialist I in a leading Biopharmaceutical company located in Santa Monica, CA.
Responsibilties include but are not limited to:
- Perform all activities around scanning and archiving documents for the site
- Performs a variety of activities to ensure compliance with applicable regulatory requirements.
- Performs basic administration tasks supporting maintenance of programs and processes, to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs).
- Performs routine tasks to issue, verify batch records, scan and archive documents, with guidance from senior colleagues.
- Perform other duties as assigned
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