Manufacturing Team Leader

CatalentGreenville, NC
Onsite

About The Position

This role will be responsible for leading manufacturing team to deliver timely, accurate batch production while partnering with cross-functional teams to support operational needs. Position Summary This position is 100% on-site at the Greenville site. Shift: 4 pm - 2:30 am Monday - Thursday 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 Role Provide leadership and expertise to manufacturing team to ensure the timely and accurate completion of manufacturing operations. With close supervision, support and occasionally lead the scheduling and planning of client project work to ensure the highest level of efficiency and quality standards are met. Serve as a liaison with other functional teams to support project work requiring cross-functional support. Ensure manufacturing area and equipment are maintained in accordance with company and regulatory requirements. Serve as the Subject Matter Expert (SME) on manufacturing processes and lead on the job training for team members. Support production and completion of batches through occasionally operating machinery to manufacture scale-up, bio-batches, full production scale batches, and CTM batches. Troubleshoot machinery and equipment; Identify and resolve process and/or equipment failures, and initiate appropriate action to prevent reoccurrence. All other duties as assigned.

Requirements

  • Bachelor’s degree with at least two years of OSD manufacturing experience in the pharmaceutical industry required or; Associate degree with at least four years of OSD manufacturing experience in the pharmaceutical industry or; High school diploma or equivalent with at least six years of OSD manufacturing experience in the pharmaceutical industry required.
  • At least one-year experience in a leadership role in the pharmaceutical industry required
  • Ability to lift 40 lbs unassisted, and push and pull in excess of 100 lbs.
  • 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.
  • Employment is contingent upon being able to complete a medical evaluation with satisfactory results for respirator use.

Nice To Haves

  • Experience with inventory management systems, specifically SAP, is preferred

Responsibilities

  • Provide leadership and expertise to manufacturing team to ensure the timely and accurate completion of manufacturing operations.
  • Support and occasionally lead the scheduling and planning of client project work to ensure the highest level of efficiency and quality standards are met.
  • Serve as a liaison with other functional teams to support project work requiring cross-functional support.
  • Ensure manufacturing area and equipment are maintained in accordance with company and regulatory requirements.
  • Serve as the Subject Matter Expert (SME) on manufacturing processes and lead on the job training for team members.
  • Support production and completion of batches through occasionally operating machinery to manufacture scale-up, bio-batches, full production scale batches, and CTM batches.
  • Troubleshoot machinery and equipment; Identify and resolve process and/or equipment failures, and initiate appropriate action to prevent reoccurrence.

Benefits

  • 152 hours of PTO + 8 paid holidays
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