Biopharm Manufacturing Associate (Entry Level)
$45,760–$47,840 year
On-siteKing of Prussia, Pennsylvania, United States
Job Summary
Execute daily manufacturing activities by following Standard Operating Procedures (SOPs) and batch records while accurately documenting all operations in accordance with GMP requirements. Dispense small and large quantities of raw materials, perform Cleaning-in-Place and Sterilization-in-Place of equipment and product tanks, and assist with troubleshooting manufacturing processes. Author, revise, and support SOPs, deviations, and change controls while safely handling hazardous materials using established safety procedures. Support continuous improvement initiatives and collaborate across cross-functional teams within an upstream manufacturing environment. This 12-month contract position in King of Prussia, PA, requires a Bachelor's degree in a scientific discipline and familiarity with GMP regulations.
Required Qualifications
- Bachelor's degree in Biology, Chemistry, Chemical Engineering, or another scientific or engineering discipline
- Familiarity with Good Manufacturing Practices (GMP)
- Strong written communication and documentation skills
- Computer proficiency
- Ability to follow detailed written procedures
- Strong problem-solving and troubleshooting abilities
- Ability to work effectively in a collaborative, fast-paced environment
- 100% onsite position based in King of Prussia (Upper Merion), PA
- Initial 12-month contract with the potential to extend up to 18 months based on business needs and performance
- This is an Upstream Manufacturing role supporting biopharmaceutical production
- Candidates must be able to wear a Powered Air-Purifying Respirator (PAPR) as required for the position
- Following hire, candidates will complete a medical clearance/respirator screening in accordance with OSHA requirements before using a PAPR (Non-SCBA)
Desired Qualifications
- 1+ year of cGMP or pharmaceutical manufacturing experience
- Knowledge of GMP regulations and documentation practices
- Experience with upstream manufacturing processes, including media preparation and bioprocess unit operations
- Familiarity with analytical equipment such as: Vi-Cell, NOVA Analyzer, Centrifuges, Tubing Welders
- Exposure to PLC, DCS, or HMI systems
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