Technician - Biomanufacturing, Central Services
Catalent
Summary
This is an entry level position in the Manufacturing team and is the starting point to acquiring skills and training required for a cGMP biomanufacturing environment. The Technician is responsible for the manufacture of biopharmaceutical products within a clean room environment, following detailed instructions and established procedures with frequent supervision.
Job description
Position Summary
This is an entry level position in the Manufacturing team and is the starting point to acquiring skills and training required for a cGMP biomanufacturing environment. The Technician is responsible for the manufacture of biopharmaceutical products within a clean room environment, following detailed instructions and established procedures with frequent supervision.
The Role
- Perform basic buffer preparation activities, including weighing raw materials for production
- Accurately follow manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with cGMPs with a focus on right first time execution
- Document all activities in accordance with Good Documentation Practices (GDPs) in BPRs, Forms, and other quality documentation
- Recognize deviations from the intended procedure and raise awareness through the Rapid Response process
- Proactively identify safety, quality, and efficiency improvements; actively participate in the Catalent Way (Continuous Improvement Culture)
- May lead Just Do It (JDI) Continuous Improvement activities and engage in implementation of CI projects
- May coach more junior team members on basic execution activities and act as an onboarding buddy
- Perform general cleanroom housekeeping, including room and equipment cleaning, disposal of waste, and maintenance of 5S standards
- Other duties as assigned
The Candidate
- Must have High School Diploma or equivalent; no additional experience required
- GMP manufacturing experience preferred
- Ability to use Microsoft Word and Excel, and other Office systems
- Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software
- Physical requirements include frequent sitting, standing, walking, reading, reaching, talking, writing, listening; occasional stooping, kneeling, crouching, bending, carrying, grasping; frequent lifting up to 10 pounds and occasional lifting up to 50 pounds
- Must comply with EHS responsibilities; ability to operate within a clean room environment as needed
Requirements
- High School Diploma or equivalent
- No additional experience required
- GMP manufacturing experience preferred
- Ability to use Microsoft Word and Excel and other Office systems
- Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software
- Ability to operate within a clean room environment
- Ability to lift up to 50 pounds occasionally
Benefits
- 152 hours PTO
- 8 paid holidays
- 401(k) Matching
- Medical, Dental & Vision
- Tuition Reimbursement
- Career Growth Opportunities
- Annual Performance Reviews
Company overview
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) that serves as a trusted partner to pharmaceutical, biotech, and consumer health companies worldwide. Founded on a legacy dating back to 1933, Catalent has evolved into a comprehensive drug development and delivery leader with over 40 global sites. The company specializes in providing end-to-end solutions spanning oral dose formulations, biologics, specialty products, and clinical supply services. Catalent's expertise includes formulation development, analytical services, commercial manufacturing, and advanced delivery technologies such as Zydis® fast-dissolve tablets and softgel technologies. With over 1,000 active development programs at any given time, the company launches more than 100 new products and line extensions annually and has supported half of all FDA approvals over the past decade. Catalent produces over 60 billion treatment doses per year, helping approximately 200 million patients annually. Headquartered in Tampa, Florida, the company employs more than 10,000 professionals globally who are dedicated to putting patients first and championing the missions that matter in healthcare innovation.