What can you expect as a freelance consultant at Normec Advipro? 

 At Normec Advipro, we value your extensive experience in life sciences to lead, support, and manage key projects within life sciences: 

• You'll work with leading companies in pharmaceuticals and biotechnology.
• Depending on your expertise and interests, you will take on large, complex projects in departments like QA, Engineering, Validation and Qualification.
• You stay updated on international regulations, guidelines, and industry advancements.
• You approach challenges with a solution-driven, pragmatic mindset.

Who are we looking for ? 

• You have extensive experience in industries such as pharmaceuticals, biotech, medical devices, cosmetics, or healthcare. 
• You're well-versed in GxP regulations, ISO standards, and industry guidelines (FDA, Eudralex, MDR, MHRA, FAGG, ICH, ISPE, PIC/S, etc.). 
• You excel in one or more of the following areas: 
  • CQV (Commissioning, Qualification & Validation) of Production Equipment 
  • CQV (Commissioning, Qualification & Validation) of Lab Equipment 
  • Sterilisation validation 
  • Cleanroom expertise
  • Quality Assurance
• You're a strong communicator, fluent in both Dutch and English (additional languages are a plus). 

Why choose Normec Advipro? 

• We offer tailored support, ensuring compliance with legal and regulatory requirements. 
• At Normec Advipro, you’ll form lasting, meaningful connections as part of our A-team. 
• We foster continuous learning and professional growth. 
• As an ambitious and dynamic company, we strive to provide the best environment for you to thrive in the life sciences.