Pharmaceutical Production Supervisor
7 days ago
Catalent Inc is a leading global provider of development and manufacturing services for the pharmaceutical industry.
With over $100M in recent investments, our state-of-the-art facility in Greenville, N.C. offers fit-for-scale capacity with potent handling capabilities ideal for orphan or targeted drug development.
We are committed to a Patient First culture through excellence in quality and compliance, ensuring the safety of every patient, consumer, and employee.
The Pharmaceutical Production Supervisor - Operations Lead will oversee commercial products and large-scale clinical trial material production, packaging, labeling, and shipping.
This role requires planning and supervising activities related to production and packaging while ensuring cost-effectiveness and adherence to cGMP and DEA requirements.
This is a second shift position working Monday - Thursday from 4 pm - 2:30 am.
Key Responsibilities:- Supervise and assist in successful manufacturing of commercial and large-scale clinical batches
- Maintain production schedules and timelines
- Ensure manufacturing and packaging area and equipment meet company and regulatory requirements
- Audit and revise procedures used by operative staff and ensure proper following
- Support execution of validation protocols for process and equipment validation
- High school diploma or equivalent with 7 years of relevant experience in a pharmaceutical production area, including leadership experience
- Ability to lift in excess of 50 lbs unassisted
- Majority of work day is performed while standing, walking, lifting, pulling, pushing
- Requires bending, squatting, reaching, pushing, climbing
- Ability to communicate effectively using speech, vision, and hearing
- Requires use of hands for simple grasping and fine manipulations
- Requires ability to stand for extended periods of time
- Competitive medical benefits and 401K
- 152 hours of PTO + 8 Paid Holidays
- Dynamic, fast-paced work environment
- Opportunity to work on Continuous Improvement Processes
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