Manufacturing Production Operator
About The Position
The Manufacturing Production Operator is responsible for cleaning equipment as well as dispensing, sifting, and blending of good manufacturing practice (GMP) commercial batches in an oral solid dosage (OSD) environment. Position Summary This position is 100% on-site at the Greenville site. Shift: Monday - Thursday 4 pm - 2:30 am 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.
Requirements
- High school diploma or equivalent with at least 1 year of manufacturing or related experience or completion of Grads2Work Program or BioWorks certificate program required.
- Required to obtain internal forklift operation certification.
- Position requires the ability to lift 50 lbs unassisted, and push and pull in excess of 100 lbs.
- Majority of work day is performed while standing and walking.
- Requires the use of hands for simple grasping and fine manipulations.
- Ability to occasionally bend, stoop, twist, and have full range of motion in upper and lower extremities.
- Exposure to hazardous chemicals, other active chemical ingredients, dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments.
- Must be able to use a variety of tools, equipment, and machinery.
- This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results.
- The medical evaluation is conducted via an external vendor assigned by Catalent.
Responsibilities
- With close oversight, operate equipment needed to dispense and sift scale-up, bio-batches, full commercial scale batches, and CTM batches
- Ensure all batch records and logbook entries are accurately documented and compliant with SOPs and FDA cGMP guidelines
- Assist with setup, manufacturing, and changeovers with adherence to SOPs and safety requirements
- All other duties as assigned.
Benefits
- Competitive medical benefits and 401K
- 152 hours of PTO + 8 Paid Holidays
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees
