Pharmaceutical Technician II

Catalent Pharma SolutionsGreenville, NC
Onsite

About The Position

Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market. We have an opportunity for a Pharmaceutical Tech II to join our team. In this role, you will work with manufacturing equipment, ensuring compliance with safety and quality standards. You will handle setup, changeover, and troubleshooting activities while maintaining accurate documentation. This position is ideal for someone who enjoys hands-on work in a dynamic pharmaceutical environment. Shift: Monday-Thursday 4pm - 2:30am. Hourly position. Location: Greenville, NC 100% Onsite

Requirements

  • High school diploma or equivalent with at least 3 years of experience in pharmaceutical oral solid dose manufacturing; OR Associate degree with at least 2 years of experience in pharmaceutical oral solid dose manufacturing
  • Proficiency with manufacturing skills, processes, and equipment knowledge to serve as a trainer and provide specific technical training with minimal guidance
  • Required to obtain internal forklift operation certification
  • This position requires wearing a respirator for safety; employment is contingent upon completing a medical evaluation with satisfactory results conducted by an external vendor assigned by Catalent

Responsibilities

  • Independently assemble, disassemble, clean, and store manufacturing equipment
  • Troubleshoot machinery and equipment and recommend corrective or preventative measures
  • Ensure all batch records and logbook entries are accurately documented and compliant with Standard Operating Procedures and FDA current Good Manufacturing Practice guidelines
  • Monitor operations for deviations, mechanical issues, and quality assurance
  • Conduct setup, changeover, and manufacturing activities with adherence to Standard Operating Procedures and safety requirements
  • Escalate and work to resolve any production, quality, or safety issues

Benefits

  • Competitive Paid Time Off plus 8 paid holidays
  • Medical, dental, and vision benefits effective day one of employment
  • Tuition Reimbursement
  • Site-based Employee Engagement activities
  • Employee Resource Groups focusing on Diversity and Inclusion
  • Environmentally friendly, community engagement green initiatives
  • Defined career path and annual performance review and feedback process with potential for career growth
  • WellHub program promoting overall physical and mental wellness including onsite fitness center
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