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Senior QP Compliance

Interesting position for professionals with a analytical / pharmaceutical background and a strong drive to be involved in the product development process, including the submission and approval of new products.

Job description

In this role you will play a key role in handling compliance documents within the quality center, ensuring that that the products that are being sold on the international market follow GMP / GDP guidelines.

Responsibilities

  • Ensure that the batch documentation is in accordance with GMP guidelines for NL and international markets
  • Develop and improve systems for change controls, CAPAs and deviation management
  • Update and maintain quality agreements with suppliers and customers

Profile

  • Degree in pharmacy, analytical chemistry or pharmaceutical chemistry
  • 5+ years of working experience
  • Excellent communication skills, and a team player attitude
  • Good project management skills
  • Fluency in English (Dutch is a plus)

Benefits

  • Employment: temporary contract with Oxford
  • Salary indication: from €3500
  • Working hours: 40 hours per week (part-time can be discussed)
  • Location: Amsterdam region

Vacancy number: 15657