At Halden Pharma, you'll be part of a passionate team that believes in collaboration, continuous improvement, and having fun at work. Here, your ideas matter, and your contribution will help shape the future of our products and processes.

What you'll do

Take the lead on validation and qualification of equipment, cleanrooms, and processes for exciting customer projects.
Work closely with colleagues from QC, Production, Engineering, and more - we believe the best results come from teamwork!
Prepare and update validation plans, protocols, and reports, and help us stay ahead of regulatory requirements.
Support audits and inspections, and play a key role in improvement projects across the company.

Who you are

You have a Master's degree (or similar) in engineering, chemistry, biology, pharmacy, or a related field.
You bring experience with validation in a regulated industry (pharma, medical devices, or similar).
You know your way around GMP and relevant standards (EU/FDA cGMP, ISO13485, etc.).
You're analytical, solution-oriented, and thrive in a collaborative environment.
You communicate confidently in English, both written and spoken.

What we offer

The opportunity to further develop a function that is critical to our operations
A diverse and international workplace with colleagues from over 40 nationalities
A culture built on collaboration, high standards and strong professional pride
Opportunities for both personal and professional growth

Please contact Department Manager, Anushya Gopal if you have any questions related to the position: Anushya.Gopal@halden-pharma.com

Applicants will be considered on an ongoing basis.

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