QUALIFICATIONS:

• B.S./M.S. in Biomedical Engineering, Chemical Engineering, or related discipline
• Strong observational and documentation skills
• Prior exposure to cleanroom or cGMP environment preferred
• Able to work non-standard shifts (nights, weekends)
• No known Beta-Lactam allergies

• Monitor key process parameters and assist in data interpretation
• Assist in equipment troubleshooting, process investigations, and minor calibrations
• Write and revise technical documentation and participate in internal audits
• Maintain compliance with GMP and safety regulations
• Support manufacturing readiness for tech transfers and new product introductions
• Provide shift coverage and respond to on-the-floor issues in real time