Gmp Production Supervisor

4 days ago

Nottingham, United Kingdom Catalent Full time

Catalent are currently recruiting for a **GMP Production Superviso**r to join the **Nottingham** site. The** GMP Production supervisor** will be responsible for directing manufacturing staff to ensure the timely delivery and Right First-Time execution of manufacturing operations for development projects and manufacturing batches.

**The Role**:

- To manage the ‘hands-on’ day-to-day running of the Production area to ensure all operations are undertaken and facilities maintained in accordance with company Quality Management System and Standard Operating Procedures (SOP's).
- Support the Clinical Manufacturing Management team, undertaking direct supervision of Pharmaceutical Operators within the GMP Manufacturing Facility ensuring that all clinical manufacturing activities are undertaken to a high standard of quality in accordance with exemplary Good Manufacturing Practice (cGMP) across a full range of dosage forms (solid, semi-solids, solutions, suspensions, ointments and creams).
- Daily compliance checks of Batch documentation, equipment and facility logbooks to ensure continual compliance.
- Ensuring tasks are undertaken and completed in full and in a compliant manner in line with scheduled activities as directed by GMP Production Manager.
- cGMP compliance activities related to manufacturing equipment, documentation and facilities
- Cross functional collaboration with Validation, Quality Assurance, Analytical Services, Engineering, and Project Management functional areas to plan and implement the execution of cGMP activities in Manufacturing Operations for both development processes and commercial operations.
- Ensure timely and compliant GMP room clean-down/cleaning verification activities undertaken.
- Ensure all key processing equipment are appropriately validated and calibrated to meet GMP Manufacturing needs.
- Ensure compliant GMP Facility, including, but not limited to Management of the Environmental Monitoring System (EMS), investigation and reporting of out of specification incidents.
- A minimum of 5 years’ experience in a GMP Pharmaceutical Manufacturing environment, preferably across a broad range of dosage forms, with some supervisory experience.
- Strong GMP Compliance experience.
- 2 years + line management experience.

**Position Benefits**
- Annual Salary
- Annual Bonus
- Shift Allowance
- Pension
- Healthcare
- Life Assurance

**Catalent offers rewarding opportunities to further your career** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

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