Senior Associate Quality

Discipline: Biotechnology
Job type: Temporary/Freelance
Contact name: Benjamin Watts

Contact email:
Job ref: 13624
Published: about 1 month ago

I am looking for a Sr. Associate Quality – Internal Distribution to join a leading biotechnology company.


  • Provide regional support to ensure that quality system is implemented and maintained to ensure medicinal products are procured, held, supplied in a way that is compliant with the requirements of GDP
  • Provide regional support to initial and continuous training programs are in place, and accordingly maintained
  • Act as Subject Matter Expert (SME) on Training matters within the region, and towards the network
  • Execute Training Impact assessments within the validated Document Management System
  • Perform Training assessments as part of the document creation, revision or obsoletion within the validated Document Management System
  • Process online Training requests for new training assignments, updates on existing trainings, etc.
  • Ensure regional and local Training Assignment Portfolios exist and are kept up to date
  • Maintain IDQ onboarding manual
  • Act as SME on Document Management System (DMS) within the region, and towards the network
  • Act as SME on Commercial Temperature Excursions within the region, and towards the network
  • Assess any temperature excursion occur during transport
  • Participate in initiatives involving Commercial Temperature Excursions process improvements and updates
  • Provide support to the Regional and Global SME in Product Complaints
  • Provide support to the region during the deployment of Product Complaints process changes and update

Education and Experience Requirements:  

  • Bachelor or MSc degree in Life sciences or related field education
  • Deep understanding of Global Regulatory guidelines (Good Distribution Practice and Good Manufacturing Practice) with the ability to interpret and apply in both routine and non-routine cases
  • Knowledge of warehouse and distribution processes of Medicinal products, in conjunction with sound knowledge of Quality Assurance principles
  • Strong word processing, database and spreadsheet application skills
  • Fluency in English, and any additional language will be a plus

Project start date: ASAP  

Project Duration: 1 year (highly extendable)  

Location: Breda


If you’re interested in the above description, please apply with your CV.

PS: Did you also know that we offer a generous referral scheme, because great people know other great people, right?

For further information, please contact Benjamin Watts at +31 (0)20 20 44 502 or by email at