Manufacturing Equipment Specialist II

Position Summary

• 100% on-site in Greenville, NC
• Work Schedule:
  
  2nd shift

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.

• Location:
  
  Greenville, NC
• Shift: 2nd shift

• Equivalent experience as Manufacturing Equipment Specialist I
• Demonstrates the ability to work with minimum to no supervision.
• Provides intermediate level of knowledge related to maintaining pharmaceutical manufacturing.
• Performs maintenance, troubleshooting and repairs related to mechanical, electrical, pneumatic functions utilizing equipment manuals and support drawings related to manufacturing equipment.
• Assist with training Manufacturing Equipment Specialist I.
• Performs equipment preventive maintenance and calibration procedures.
• Compile and maintain all information and document relevant to all work under FDA guidelines.
• Coordinate repairs/installations with facilities staff, contractors and users to minimize interruptions.
• Work as part of a team with manufacturing staff, users and vendors to continuously improve operations.
• Ability to work from blueprints, drawings, layouts or other specifications.
• Other duties assigned.

• Associate degree in technical or life sciences discipline with at least 5 years of mechanical experience or high school diploma or equivalent with at least 7 years of mechanical experience required.
• At least 2 years Manufacturing Equipment experience.
• Good understanding of cGMPs, industry and regulatory standards and guidelines.
• Good understanding of federal and local regulations regarding health and safety within manufacturing and packaging environments.
• Ability to lift in excess of 50 lbs unassisted.
• 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.

• Competitive medical benefits and 401K.
• 152 hours PTO + 8 paid holidays.
• Dynamic, fast‑paced work environment.
• Opportunity to work on continuous improvement processes.

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.

Personal initiative. Dynamic pace. Meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation. Include the job number, title and location to Disabili This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.