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GMP Facility Design Consultant (Fractional), Confidential

This role supports GMP-compliant manufacturing projects, focusing on facility design, evaluation, and planning for biologics production. The work involves reviewing technical documentation and advising on facility decisions.

About The Role

This is a part-time, remote consulting role starting at around 8 hours per week, with the potential to increase to 15 hours.

You will support CDMO evaluation and facility design decisions, providing input on manufacturing environments and compliance requirements.

What You Will Do

You will review CDMO documentation, including proposals, facility layouts, material flow, and build-out plans. You will assess scalability and ensure alignment with GMP standards.

You will participate in team discussions, provide input on planning decisions, and offer guidance on facility design and compliance considerations.

Who You Are

You have experience in biotech manufacturing facilities, particularly in design and engineering for biologics production. You understand GMP requirements and how they apply to facility setup and operations.

You are comfortable reviewing technical documentation and providing clear input to support decision-making. Experience with viral vector manufacturing or utilities is a plus.

Additional Information

This is a remote role with an initial commitment of around 8 hours per week, with potential to increase based on project needs.

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