Cipla
Job Title: QA Document Control Specialist
Organization Name: InvaGen Pharmaceuticals
Location: 550S Research Place, Central Islip, NY 11722
Work Hours/Shift: In Office 8:30 AM - 5:00 PM
Responsibilities
Work with manager to determine which documents must be packed up and which will stay.
Organize the locations in the room for various documents for all three units.
Index the contents of the room for easy retrieval during inspections or reviews.
Box up older documents for off-site storage at Iron Mountain.
Update the index daily based on incoming documents.
Maintain logs of document movements and storage.
Coordinate with Iron Mountain for document pick-up and retrieval.
Review the index during inspections or department reviews to locate requested documents.
Notify departments upon receipt of requested documents.
Log out documents being removed and obtain signatures.
Support during FDA inspections or audits as needed.
Perform other duties as assigned.
Qualifications Education: AS degree or equivalent experience in pharmaceutical or Life Sciences documentation. Experience: 1-3 years in Quality Assurance with documentation systems within a pharmaceutical cGMP environment preferred. Must be able to read and speak English.
Additional Information
Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industry: Pharmaceutical Manufacturing
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Qualifications Education: AS degree or equivalent experience in pharmaceutical or Life Sciences documentation. Experience: 1-3 years in Quality Assurance with documentation systems within a pharmaceutical cGMP environment preferred. Must be able to read and speak English.
Additional Information
Seniority level: Entry level Employment type: Full-time Job function: Quality Assurance Industry: Pharmaceutical Manufacturing
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