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QC coordinator Raw Materials

We have an exciting new opportunity for QC professionals in the pharmaceutical industry! Are you looking for a new challenge at an international company? In this role you will be key player in coordination of new product intruction, quality of raw materials and analytical method transfer. Apply now.

Job Description

For one of our clients within pharmaceutical industry we are looking for a QC specialist with expertise in the field of raw materials. In the dynamic raw materials team you will contribute to new product introduction (NPI) activities in relation to raw material qualification. You will coordinate analytical method transfer, review quality documentation, lead continious improvement projects, adhere to compliance with GMP and EHSS regulations, and lead NPI deviations. With you analytical expertise you judge new technologies and coordinate the process of making tests ready for QC laboratory testing. Whenever a new product is introduced you ensure its robustness en reliability, but whenever there is a non-conformancy you take the appropriate actions. We are looking for a pro-active and motivated professional that can contribute to improvement projects and works well with deadlines.

Responsibilities

  • Coordination of raw material sample handling and testing for both new and qualified materials;
  • Handling quality events related to raw material testing;
  • Reviewing documentation and test results before release of raw materials for commercial use;
  • Meet business needs by introducing new raw materials and qualifying new sources of existing materials;
  • Participate in meetings with various stakeholders in the context of your NPI project;
  • Taking the lead in deviations, non-conformaces and coordinate CAPA's;
  • End-to-end analytical method transfer;

Requirements

  • BSc or MSc in analtytical chemistry or equivalent;
  • A minimum of 3 years of work experience is required, preferably in the pharmaceutical or biotechnology industry (starters do not qualify);
  • Extensive know-how on pharmaceutical raw materials and associated regulations;
  • Experience working in a strictly regulated environment such as GMP or GLP;
  • A team player, pro-active and result-oriented;
  • English is a Must, Dutch is considered a plus;
  • Located in the vicinity of Leiden;
  • Valid Dutch work permit is a must, candidates not in possession of a work permit will not receive a response;

Benefits

  • Contract: 1 year via Oxford, realistic long- term perspective;
  • Salary: €3000- €4000 gross monthly based on a full-time position;
  • Holidays: 25;
  • Working hours: full-time, 32 hours possible;
  • Region: Leiden;
  • Vacancy number: 20480;