Senior Process Development Engineer – Nuclear Pharmaceuticals

Introduction

Are you ready to play a leading role in developing the next generation of nuclear pharmaceutical products? In this challenging position, you will scale innovative manufacturing processes from laboratory development to robust, GMP-compliant production. You will work in a high-tech environment where innovation, quality and radiation safety are equally important. Together with multidisciplinary experts, you will contribute to groundbreaking solutions that make a meaningful impact on global healthcare.

Your Responsibilities

You will be responsible for developing, optimizing and safeguarding robust manufacturing processes for innovative pharmaceutical products.

• Lead technology transfers from R&D to GMP manufacturing.
• Develop process descriptions, process flow diagrams and process documentation.
• Conduct and facilitate structured process risk assessments, including pFMEA and MRA.
• Define process validation strategies and establish process knowledge, CPP and CQA control strategies based on QbD principles.
• Support deviation investigations, root cause analyses, CAPAs and continuous process improvements.

Company Profile

You will join an innovative organization within the nuclear pharmaceutical industry that is dedicated to developing diagnostic and therapeutic radioisotopes. As part of an organization with more than 500 employees, you will work in a multidisciplinary team of approximately 25 professionals, including scientists, process engineers and project managers. The culture is collaborative, innovative and driven by an uncompromising focus on quality and safety. Here, you will have the opportunity to shape technologies that improve the lives of patients around the world.

Your Profile

• Bachelor's or Master's degree in Chemical Engineering, Process Engineering, Pharmaceutical Technology or a related discipline.
• Extensive experience in process development, technology transfer or process optimization within the pharmaceutical industry.
• Strong knowledge of GMP, quality systems and pharmaceutical regulations.
• Experience with process validation, QbD, FMEA, scale-up and complex manufacturing environments.
• Excellent analytical and problem-solving skills with a structured approach and strong focus on quality and safety.
• Nice to have: proficiency in the Dutch language.

Don't meet every requirement but still see yourself in this role? We'd still love to hear from you!

What We Offer

• A gross monthly salary between €4,750 and €7,500.
• 27 vacation days and 12 ADV (additional leave) days, or the option to receive an additional 5.26% salary instead.
• 8% holiday allowance, an 8.3% year-end bonus and an excellent pension scheme with 70% of the premium paid by the employer.
• Travel reimbursement or full public transport reimbursement, with additional options for a mobility budget or relocation assistance.
• A comprehensive onboarding programme, extensive learning and development opportunities, an active staff association and an inspiring working environment.

Interested?

Are you excited about this opportunity or would you like to know more? Apply today or contact Benthe Berting by phone/WhatsApp: +31 (0)6 190 28 768 or email: [email protected]