Process Development Consultant

Eligibility Requirement: Candidates must hold valid rights to work in the EU/Belgium.

Assignment Purpose

Support the transfer and scale‑up of new processes between R&D and manufacturing. Provide technical expertise, project leadership, and cross‑functional coordination to ensure smooth integration of innovations into production.

Scope of Work

• Act as a technical liaison between R&D and manufacturing teams.
• Review and interpret scientific concepts, translating them into practical, scalable production methods.
• Assess mechanical process steps, equipment capabilities, and scale‑up challenges.
• Provide advisory input on chemistry aspects to support process understanding.
• Lead or support project planning, timelines, and resource coordination.
• Identify risks and propose mitigation strategies during process transfer.
• Ensure documentation, SOPs, and validation protocols align with GMP and regulatory requirements.
• Facilitate clear communication across scientific, technical, and operational stakeholders.

Consultant Profile

• Advanced degree in Chemical Engineering, Mechanical Engineering, Pharmaceutical Sciences, or related discipline.
• Demonstrated experience in process development, tech transfer, or MS&T within GMP environments.
• Strong grasp of mechanical process operations; working knowledge of chemistry preferred.
• Proven track record in project management and cross‑functional collaboration.
• Familiarity with regulatory compliance and validation standards in pharma/biotech.

Key Competencies

• Independent, self‑directed, able to deliver results within defined project scope.
• Strong communicator, capable of bridging scientific and operational perspectives.
• Analytical and solution‑oriented, with attention to detail and compliance.
• Flexible and adaptable to changing project priorities.

Engagement Details

• Duration: Fixed‑term project (e.g., 6-12 months, renewable depending on pipeline needs).
• Location: On‑site presence required for manufacturing/R&D interface, with flexibility for remote documentation and planning tasks.
• Deliverables: Successful transfer of new processes into manufacturing, validated documentation, and cross‑functional alignment.