Global Small Molecule Tech Transfer Lead

SIRE LIFE SCIENCES

Boxmeer

On-site

EUR 120,000 - 180,000

Full time

4 days ago
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Job summary

SIRE LIFE SCIENCES is seeking an Associate Director, Technology Transfer Execution to lead Small Molecule technology transfer programs across global manufacturing sites. You will guide planning, execution, and delivery in compliance with GMP and regulatory standards while coordinating with Manufacturing, Quality, Regulatory Affairs, Supply Chain, and CMOs.

The role requires a Bachelor’s degree in a technical field, 10+ years in technology transfer or related operations in pharma, strong project

Qualifications

  • Bachelor’s degree in Engineering, Chemistry, Biology, or related field.
  • 10+ years of technology transfer, development, or manufacturing ops in pharma.
  • Strong knowledge of GMP and EU/FDA regulatory requirements.
  • Experience with technology transfer, process validation, qualification, change control, and deviations.
  • Excellent English communication, negotiation, and influencing skills.

Responsibilities

  • Lead and coordinate multiple Small Molecule technology transfer projects across manufacturing sites.
  • Manage project timelines, milestones, risks, deliverables, and governance.
  • Coordinate donor and receiving sites and align stakeholders.
  • Cross-functionally work with Manufacturing, Quality, Regulatory, Supply Chain, and Technical teams.
  • Support GMP compliance, process validation, qualification, change controls, deviations, and regulatory documentation.
  • Travel internationally approximately 10–20% of the time.

Skills

Project management
Stakeholder management
English communication
Negotiation
Influencing skills

Education

Bachelor’s degree in Engineering, Chemistry, Biology, or related field

Tools

MS Project
Microsoft Office
SAP

Job description

SIRE LIFE SCIENCES is seeking an Associate Director, Technology Transfer Execution to lead Small Molecule technology transfer programs across global manufacturing sites. You will guide planning, execution, and delivery in compliance with GMP and regulatory standards while coordinating with Manufacturing, Quality, Regulatory Affairs, Supply Chain, and CMOs.

The role requires a Bachelor’s degree in a technical field, 10+ years in technology transfer or related operations in pharma, strong project

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