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

If you're passionate about science and ready to launch your career in pharmaceutical manufacturing, we'd love to hear from you!