Biopharm Manufacturing Associate (Entry Level)

Make Your Mark with a Job at Alphanumeric Job Details Biopharm Manufacturing Associate (Entry Level) King Of Prussia,PA Posted:7/22/2026 Job Description Job ID#: 8399 Biopharm Manufacturing Associate (Entry Level) King of Prussia, PA (Upper Merion) Alphanumeric is hiring a Biopharm Manufacturing Associate Pay Rate: $22.00-$23.00/hour Launch Your Career in Biopharmaceutical Manufacturing Are you a recent science graduate looking to break into the pharmaceutical industry? This is an excellent opportunity to gain hands-on experience in a GMP-regulated manufacturing environment while working alongside experienced professionals supporting the production of innovative therapies. No prior pharmaceutical manufacturing experience is required-just a strong scientific foundation, attention to detail, and a willingness to learn. What You'll Do As a Biopharm Manufacturing Associate, you'll support daily manufacturing operations while ensuring products are produced safely, accurately, and in compliance with GMP regulations. Responsibilities include: Execute daily manufacturing activities by following Standard Operating Procedures (SOPs) and batch records. Accurately document manufacturing activities in accordance with GMP requirements. Dispense both small and large quantities of raw materials. Perform Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) of manufacturing equipment and product tanks. Assist with troubleshooting equipment and manufacturing processes. Author, revise, and support SOPs, deviations, and change controls. Operate within a highly regulated GMP manufacturing environment while maintaining quality and compliance standards. Safely handle hazardous materials using established safety procedures. Support continuous improvement initiatives and collaborate across cross-functional teams. Perform additional manufacturing duties as assigned. Job Requirements What We're Looking For 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 Preferred 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 Work Environment & Additional Information 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) Why Join Us? Entry point into the pharmaceutical and biotechnology industry Hands-on GMP manufacturing experience Work with an industry-leading global biopharmaceutical company Collaborative, team-oriented environment Opportunity to develop valuable technical and manufacturing skills Potential for long-term career growth within biopharmaceutical manufacturing Excellent opportunity to gain hands-on upstream biopharmaceutical manufacturing experience with a global pharmaceutical leader. #J-18808-Ljbffr alphanumeric