Senior Technical Transfer Specialist

About the Role:

We’re seeking a Senior Technical Transfer Specialist to join our client’s dynamic Engineering team. You’ll play a pivotal role in the technology transfer of vaccine manufacturing processes, ensuring efficient, high-quality, and timely delivery. This is your opportunity to lead exciting technical projects within a cutting-edge biopharmaceutical environment.

Why Join Our Client?

You’ll be part of a global network striving for excellence in technology transfers and process improvements. Collaborate with colleagues worldwide and drive innovation in vaccine and biopharmaceutical manufacturing.

Key Responsibilities:

• Lead and manage the technical transfer and scale-up of new processes into the Vaccines IPT.
• Ensure compliance with the highest standards of quality, safety, and regulatory requirements.
• Facilitate production planning and execution to maintain supply of high-quality products.
• Review, own, and approve change control, quality notifications, deviations, and investigations.
• Benchmark new technologies to drive process improvements and innovation.
• Build and maintain strong relationships with cross-functional teams and stakeholders.

Your Skills and Experience:

• Honours Degree or Masters in Science or Engineering (preferably Biotechnology).
• 6+ years of experience in biopharmaceuticals/vaccines, with project leadership experience.
• Knowledge of regulatory standards and quality systems in a GMP environment.
• Strong problem-solving and facilitation skills, with experience in Lean/Six Sigma principles.
• Proven ability to manage stakeholders across diverse teams.

Why Apply?

This is more than a role—it’s a chance to shape the future of healthcare innovation while advancing your career in a supportive, forward-thinking organisation.

If you’re ready to make a difference in a fast-paced, world-class facility, apply today!

Our client is committed to diversity, inclusion, and flexible working to support your success.

Please note: You must be able to work in the Ireland or the EU without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at jkirlew@i-pharmconsulting.com or call: 

(NL)