Pharmaceutical Operator I

Catalent•Greenville, NC

3d•Onsite

About The Position

Pharmaceutical Operator I Position Summary 100% on-site Catalent 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. 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. 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. The Pharmaceutical Operator I is an entry level position in Pharmaceutical Development. This position is primarily responsible for performing manufacturing of Development and CTM batches with close supervision.

Requirements

High school diploma or equivalent
Position requires the ability to lift in excess of 50 lbs unassisted
Majority of work day is performed while standing, walking, lifting, pulling, pushing
Requires the use of hands for simple grasping and fine manipulations
Requires bending, squatting, reaching, pushing, climbing
Requires the ability to stand for extended periods of time
Some exposure to hazardous chemical and other active chemical ingredients
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.

Nice To Haves

At least 1 year of manufacturing or related experience preferred

Responsibilities

With close supervision, assist in the manufacture of development and CTM batches
With close supervision: assemble, disassemble, clean and store manufacturing equipment
Ensure that all work is accurate, precise, properly documented, compliant with SOPs and FDA cGMP guidelines
With supervision, document batch manufacturing in batch records accurately and completely as required
Perform and witness manufacturing steps
Perform, document, and witness breakdown and cleaning of process equipment, including storage.
Ensure communication with CV group and Scientific Staff.

Benefits

152 hours of PTO + 8 paid holidays
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.

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