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: depending on experience and education
Working hours: 40 hours per week (part-time can be discussed)
Location: Amsterdam region
Vacancy number: 15657
