Technician - Biomanufacturing, Central Services
About The Position
This entry-level role on the Manufacturing team provides the skills and training needed to work in a cGMP biomanufacturing environment. The Technician manufactures biopharmaceutical products in a cleanroom, following detailed instructions and established procedures with frequent supervision. The Madison, Wisconsin facility is an advanced GMP biomanufacturing site that uses single-use systems and provides integrated formulation and analytical services. The role includes basic buffer preparation and weighing raw materials, following manufacturing records and procedures, documenting work in quality records, and maintaining cleanroom housekeeping and 5S standards. The Technician also identifies and escalates deviations, participates in safety, quality, and continuous-improvement activities, and may support onboarding or coach more junior team members. The position is 100% on-site, with a 6 a.m.–4 p.m. schedule available Sunday–Wednesday or Wednesday–Saturday. Working conditions are heating, ventilation, and air-conditioning controlled, and the employee must be able to work in a cleanroom as needed.
Requirements
- High school diploma or equivalent.
- Ability to use Microsoft Word, Excel, and other Office systems.
- Ability to work in a cleanroom environment as needed and comply with applicable EHS responsibilities.
- Physical ability to frequently sit, stand, walk, read written documents, use a computer monitor, reach, talk, write, and listen; occasionally stoop, kneel, crouch, bend, carry, and grasp; frequently lift or move up to 10 pounds and occasionally lift or move up to 50 pounds.
Nice To Haves
- GMP manufacturing experience.
- Experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, or chromatography software.
Responsibilities
- Perform basic buffer preparation activities, including weighing raw materials for production.
- Follow Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with cGMPs, emphasizing right-first-time execution.
- Document activities in BPRs, forms, and other quality documentation in accordance with Good Documentation Practices (GDPs).
- Recognize deviations from intended procedures and raise awareness through the Rapid Response process.
- Identify safety, quality, and efficiency improvements and participate in the Catalent Way continuous-improvement culture.
- May lead Just Do It (JDI) continuous-improvement activities and participate in implementing improvement projects.
- May coach junior team members on basic execution activities and act as an onboarding buddy for new team members.
- Perform cleanroom housekeeping, including room and equipment cleaning, waste disposal, and maintaining 5S standards.
- Perform other duties as assigned.
Benefits
- 152 hours of paid time off and 8 paid holidays.
- Generous 401(k) match.
- Medical, dental, and vision benefits.
- Tuition reimbursement.
- Defined career path and annual performance review and feedback process.
- Potential for career growth on an expanding team.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
