Biopharm Manufacturing Associate (Entry Level)
King of Prussia, PA (Upper Merion)
Alphanumeric is hiring a Biopharm Manufacturing Associate to join our client of over 20 years, a global biopharmaceutical leader dedicated to developing life-changing medicines and improving patient lives.
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.
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.
If you're passionate about science and ready to launch your career in pharmaceutical manufacturing, we'd love to hear from you!