Project Lead Engineer

Engineer | GMP | Pharma | Biotech
Your new role
As a Project Lead Engineering, you will be responsible for leading complex engineering projects within a GMP‑regulated pharmaceutical environment. You will manage projects from concept to completion, ensuring safe, compliant, and efficient execution in both drug substance and drug product manufacturing areas. Your scope includes projects such as cleanroom reconstructions, capacity expansions, technical and efficiency upgrades, and large multidisciplinary initiatives including tech transfers. You will coordinate internal teams, external partners, and contractors, while maintaining full oversight of planning, budgeting, documentation, and stakeholder communication. You independently write and review GMP documentation, including change controls and qualification documents, and ensure all engineering activities meet FDA, EMA, and internal regulatory standards. You will provide technical leadership throughout design, installation, commissioning, and qualification of new systems and equipment. Finally, you will prepare detailed project reports, present updates to senior management, and maintain strong relationships with vendors delivering critical project components.

What you'll need to succeed
  • You have proven experience leading engineering projects in a GMP pharmaceutical setting and are comfortable navigating complex technical and regulatory environments.
  • You combine strong project management skills with the ability to collaborate effectively with multidisciplinary teams.
  • You have solid knowledge of Good Engineering Practices, GMP, and qualification/validation processes.
  • You communicate clearly, manage expectations well, and are able to work both independently and as part of larger project teams.

Your new company
Our client is an innovative pharmaceutical organisation focused on high‑quality drug substance and drug product manufacturing. Operating in a highly regulated environment, they continuously invest in technical improvements, capacity expansion projects, and state‑of‑the‑art cleanroom and facility upgrades. You will work closely with teams across engineering, production, quality assurance, and regulatory affairs, all committed to delivering safe, compliant, and reliable products that support patients worldwide.

What you'll get in return
Hays Detachering | You will start with a contract for 6 months through Hays, with an anticipated extension depending on project pipeline and performance. The position falls within schaal €5.100– €7.400 with a maximum freelance rate of €125 per hour. You will join a dynamic, highly technical environment where quality, safety, and continuous improvement are central. Travel expenses are covered. Visa sponsorship cannot be provided or supported.

What you need to do now
If you're interested in this role, click ‘apply now’ to send an up‑to‑date copy of your CV, or call us. If this job isn’t quite right for you but you’re exploring new opportunities, contact us for a confidential career discussion.

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Summary

Job type
Temporary
Industry
Pharmaceuticals
Location
Amsterdam
Specialism
Life Sciences
Pay
7400
Ref:
1049950
Closing date
1 Apr 2026

Talk to a consultant

Talk to Robbie Wootton, the specialist consultant managing this position, located in Amsterdam
Hays Amsterdam, Rijnsburgstraat 9-11

Telephone: 0202192042

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