Biopharm Manufacturing Assoc
About The Position
Biopharm Manufacturing Associate II Upper Merion (King of Prussia), PA Alphanumeric is hiring Biopharm Manufacturing Associates II to join our client of over 20 years, a global biopharmaceutical leader committed to developing life-changing medicines that improve patients' lives. Are you passionate about science, manufacturing, and making a difference? Join a collaborative manufacturing team responsible for producing innovative biologic therapies in a highly regulated cGMP environment. You'll gain valuable experience working with advanced manufacturing technologies while contributing to medicines that impact patients around the world.
Requirements
- Bachelor's degree in Biology, Chemistry, Biochemistry, Chemical Engineering, Biotechnology, or another scientific discipline with cGMP manufacturing experience OR Associate's degree in Biotechnology or a related technical field with cGMP manufacturing experience OR High School diploma/GED with at least one year of cGMP manufacturing experience
- Strong written and verbal communication skills
- Excellent attention to detail and documentation skills
- Ability to work effectively in a collaborative manufacturing environment
- Applicants must be legally authorized to work in the United States on a W-2 basis.
Nice To Haves
- Experience working in a pharmaceutical or biotechnology manufacturing environment
- Knowledge of cGMP regulations and documentation practices
- Experience with fermentation, cell culture, chromatography, filtration, or downstream manufacturing operations
- Familiarity with SAP, Electronic Batch Records (EBR), or other manufacturing systems
- Experience supporting validation, engineering, or technology transfer activities
- Demonstrated troubleshooting and problem-solving abilities
Responsibilities
- Support upstream biopharmaceutical manufacturing operations by performing production activities including fermentation, cell culture, solution preparation, filtration, chromatography, and concentration processes
- Operate and monitor automated manufacturing equipment
- Complete manufacturing tasks in accordance with SOPs, batch records, and GMP documentation requirements
- Prepare, clean, sanitize, and maintain manufacturing equipment and production areas
- Perform autoclave operations and parts washing of process assemblies
- Monitor critical process parameters and assist with troubleshooting activities
- Support engineering, validation, and technology transfer activities
- Participate in safety, compliance, deviation investigations, and continuous improvement initiatives
- Collaborate with Manufacturing, Engineering, Quality, Validation, and Technical Operations teams
- Maintain accurate documentation and data integrity in accordance with cGMP requirements
Benefits
- Competitive hourly pay
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
