Biopharmaceutical Manufacturing Associate

Proclinical; Upper Merion Township (Montgomery County); On-site; USD 52,000 - 68,000; Full time

Job summary

Proclinical seeks a Biopharmaceutical Manufacturing Associate to support large-scale production operations in Upper Merion, PA. The role involves hands-on work across fermentation, cell culture, chromatography, and related tasks, with emphasis on safety and cGMP compliance.

You will document tasks, monitor processes, and participate in investigations, with cross-functional collaboration on validation, technology transfer, and FAT, while leveraging SAP, EBR, and AR/VR tools.

Qualifications

• Biotechnology background or related field required.
• Familiarity with cGMP in a manufacturing environment.
• Ability to work effectively in a team.
• Attention to detail and ability to follow precise processing instructions.
• Competence in accurate documentation practices.

Responsibilities

• Perform and document daily manufacturing tasks following SOPs and batch instructions.
• Monitor equipment and critical process parameters to ensure optimal performance.
• Escalate issues and participate in troubleshooting and investigations as needed.
• Support cross-functional activities such as engineering validation, technology transfer, and FAT.
• Engage in continuous improvement efforts and uphold safety and compliance standards.
• Maintain proficiency with SAP, EBR, and AR/VR tools.

Skills

Teamwork

Attention to detail

Documentation practices

cGMP familiarity

Education

Biotechnology or related field background

Tools

SAP

Electronic Batch Records

AR/VR tools

Job description

Biopharmaceutical Manufacturing Associate - Contract - Upper Merion, PA

Do you have experience in biopharmaceutical manufacturing and want to play a hands-on role in producing life-changing therapies at scale?

Proclinical is seeking a Biopharmaceutical Manufacturing Associate to support large-scale production operations.

Primary Responsibilities:

This role involves working with advanced manufacturing processes, including fermentation, cell culture, solution preparation, chromatographic separations, filtration, and other related tasks. You will play a key role in ensuring compliance with safety standards and contributing to continuous improvement initiatives.

Skills & Requirements:

• Educational background in Biotechnology, a related technical field, or equivalent experience.
• Familiarity with current Good Manufacturing Practices (cGMP) in a manufacturing environment.
• Ability to work effectively in a team setting.
• Attention to detail and ability to follow precise processing instructions.
• Competence in accurate documentation practices.

The Biopharmaceutical Manufacturing Associate's responsibilities will be:

• Perform and document daily manufacturing tasks following standard operating procedures (SOPs) and batch instructions.
• Monitor equipment and critical process parameters to ensure optimal performance.
• Escalate issues and participate in troubleshooting and investigations as needed.
• Support cross-functional activities such as engineering validation, technology transfer, and factory acceptance testing (FAT).
• Engage in continuous improvement efforts and uphold safety and compliance standards.
• Maintain proficiency with digital platforms, including SAP, electronic batch records (EBR), and augmented/virtual reality tools.

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