Principal Scientist & AI-focused Development Specialist, QC (12 months temporary)

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

Do you have a practical mindset, GMP experience – and a curiosity for how AI, digitalization and automation can make QC better? Then we might have the perfect role for you. Have you ever thought, “Why are we still doing this manually?” – and then rolled up your sleeves to fix it?  If yes, you’ll feel right at home with us. Join us in QC Development and modernize QC with us - we need your hands-on skills!

This is a 12-month maternity cover.

QC Development
The QC Development team is committed to modernizing QC processes and driving innovation. We are a small, collaborative team working in an FDA-regulated CDMO, where we believe work should be both meaningful and enjoyable. 

We focus on projects we’re passionate about – and support each other in making real progress every day. As part of our mission, we explore and drive the implementation of new technologies – including AI – to improve quality, efficiency, and decision-making in QC. 

Our mission 

• Simplify processes for QC 

• Drive digitalization and automation of QC processes 

• Elevate project maturity 

• Integrate AI into QC processes 

Role & Responsibilities
This is a 12-month maternity cover with real opportunities to shape the way technology is implemented and expanded in QC. You’ll work within the area that fits your expertise and interest – whether that’s digitalization, automation, or AI. 

Some examples of your tasks: 

• Implement or improve digital solutions across QC laboratories 

• Exploring how AI can be used to simplify or support QC processes 

• Identify opportunities for process improvements and simplifications 

• Collaborate with QC teams to design user-friendly, efficient solutions 

• Translate technical concepts into clear documentation and training 

• Qualification activities (URS, risk assessments, protocols, etc.) 

• Driving cross-functional collaboration with QC, QA, and IT 

• Contributing to training, roll-out, and follow-up on new solutions 

Your Profile

We imagine you have many of the following:

• 3 years of experience from QC, QA, lab support or process development in a GMP environment 

• Experience with (or strong interest in) using AI, automation or digital tools 

• A passion for optimization, structure and finding better ways of working 

• The ability to work both independently and as part of a collaborative team 

• An open mind towards new technology and digital tools 

• Hands-on experience with process improvement, digital tools or lab automation 

• Familiarity with qualification documentation and change control processes 

• A structured approach to documentation, risk assessments and compliance 

• A proactive mindset and the ability to get thin