Biotech and Pharmaceutical, CIP (Clean-in-Place), Change Control, Continuous Improvement, Cross-Functional, Detail Oriented, Drug Manufacturing, GMP (Good Manufacturing Practices), Hazardous Materials/Substances, Identify Issues, Manufacturing, Manufacturing Equipment, Manufacturing Operations, Manufacturing/Industrial Processes, Medical Products, Operational Support, Operations, Patient Care, Procedure Development, Production Support, Quality Management, Regulatory Compliance, SIP (Sterilization-in-Place), Safety Process, Standard Operating Procedures (SOP), Writing Skills
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.
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Alphanumeric Systems Inc