Why join us?
At Halden Pharma, you'll be part of a passionate team that values collaboration, continuous improvement, and a positive work culture. Your ideas matter here, 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 - because we believe the best results come from teamwork!
• Prepare and update validation plans, protocols, and reports, ensuring compliance with regulatory requirements.
• Support audits and inspections, and play a key role in improvement projects across the company.

Who you are• You hold a bachelor`s or a Master's degree in engineering, chemistry, biology, pharmacy, or a related field.
• You have experience with validation in a regulated industry.
• You are familiar with 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• A unique opportunity to further develop a function that is critical to our operations.
• A diverse and international workplace with colleagues from over 45 nationalities.
• A culture built on collaboration, high standards, and strong professional pride.
• Opportunities for both personal and professional growth.

Interested in this position?
If you would like to know more or apply, please contact Anushya Gopal, Department Manager.
Candidates will be evaluated on an ongoing basis,