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Quality Assurance Specialist, Commercial Manufacturing - Greenville North Carolina
Company: Disability Solutions Location: Greenville, North Carolina
Posted On: 11/17/2024
Quality Assurance Specialist, Commercial Manufacturing Position SummaryCatalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.Second Shift: Monday - Thursday, 4 PM - 2:30 AM---------------------- ------------------------The Quality Assurance Specialist will perform established routine and non-routine Quality Assurance tasks with minimal supervision in support of internal non-commercial clients, external clients and/or commercial processes and projects as assigned. The Quality Assurance Specialist will perform batch record review and on the floor Quality Assurance commercial manufacturing support.Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.The Role - Review quality documentation including but not limited to review and release of batch records and/or product, release of equipment, room set up, room clearance, initial documentation of unplanned events as appropriate.
- Ensure integrity of data through accurate transactions, documentation, and tracking of all cGMP activities.
- Provide broad advocacy for the continued improvement of quality standards and the development and maintenance of a quality culture across the organization.
- Support the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standard. Perform gemba walks of manufacturing and packaging areas. Work to create an environment of open communication, participation, and information-sharing within and between teams within quality assurance and throughout the facility.
- Ensure compliance to all compendial, internal and client-specific requirements (i.e. SOPs, Quality Agreements, General and Informational Chapters in multiple compendia as applicable).
- Provide assistance to manufacturing with appropriate quality oversight. Provide real-time support activities for manufacturing and packaging.
- Escalate unplanned events and issues, providing immediate notification to QA Management, supporting and providing guidance to manufacturing staff. Demonstrate knowledge of root cause analysis techniques to support manufacturing investigation teams.
- Remain proficient and knowledgeable within respective field of operation in accordance with job responsibility and function, able to troubleshoot process, system, material and technique-related issues. Become proficient in ERP System, Document Management System and TrackWise.
- Other duties as assigned.The Candidate
- Bachelor's degree with 4+ years of professional experience in the pharmaceutical industry and 2 years in a direct QA role required OR
- Associate degree with 5+ years of professional experience in the pharmaceutical industry and 3 years in a direct QA role required.
- Must have experience with batch record review and on the floor Quality Assurance commercial manufacturing support.
- Position requires the capacity to handle and manipulate objects using hands and arms.
- Individual may be required to sit, stand, walk regularly and occasionally lift 0-20 pounds.Why You Should Join Catalent
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