Pharmaceutical Technician II

Catalent • Greenville, NC

10h • Onsite

About The Position

Pharmaceutical Technician II The Pharmaceutical Technician II is responsible for the dispensing, compounding, compressing, encapsulating, tablet coating and printing 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 three years of experience in pharmaceutical OSD manufacturing; or Associate degree with at least two years of experience in pharmaceutical OSD manufacturing.
• Demonstrated proficiency with manufacturing skills, processes and equipment knowledge to serve as a trainer to provide specific technical training on processes and equipment with minimal guidance.
• Required to obtain internal forklift operation certification.
• Position requires the ability to lift in excess of 50 lbs unassisted.
• Majority of work day is performed while standing, walking, lifting, pulling, pushing, bending, squatting, reaching, and climbing.
• Requires the use of hands for simple grasping and fine manipulations.
• 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.

Responsibilities

• Independently assemble, disassemble, clean and store manufacturing equipment
• Ability to troubleshoot machinery and equipment and recommend corrective or preventative measures
• Ensure all batch records and logbook entries are accurately documented and compliant with SOPs and FDA cGMP guidelines
• Monitor operations for deviations, mechanical issues, and quality assurance
• Conduct setup, changeover, and manufacturing activities with adherence to SOPs and safety requirements
• Escalate and work to resolve any production, quality, or safety issues
• All other duties as assigned.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees