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/hourLaunch 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 ForRequired QualificationsBachelor'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 Qualifications1+ 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 Information100% 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!