Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Quality Assurance Officer

Posted Feb 28, 2022
Job ID: JJJP00010280
Location
Leiden
Hours/week
40 hrs/week
Timeline
10 months
Starts: Mar 1, 2022
Ends: Dec 31, 2022
Payrate range
Unknown
Application Deadline: Mar 23, 2022 12:00 AM

Quality Assurance Officer

The Netherlands, 1-year contract, 32h-40h, Hybrid way of working


Johnson & Johnson Worksense is responsible for finding, engaging, and contracting talent for the Johnson & Johnson contingent workforce.

 We are currently recruiting a Quality Assurance Officer to join our contingent workforce on a growing team in Janssen Pharmaceuticals in Leiden for 12-month contract. 

In this role, you will contribute to the Quality support for all New Products and vaccine quality-related topics within the Leiden manufacturing site (i.e. development departments, production facilities, and quality control labs). You will act as a quality expert and apply the Quality Systems to create, review and approve GMP documentation. 

 

You as a Quality Assurance Officer will be responsible for:

  • Review and approve validation assessments, protocols, and reports
  • Review and approve analytical method transfer protocols and reports
  • Perform batch record review
  • Release Raw Materials
  • Provide review and approval of document changes and change controls
  • Track and monitor progress to anticipate, flag, and prevent any delays
  • Act as a member for local or global capacity/quality projects
  • Optimize current Quality Processes

 

You as a Quality Assurance Officer have:

  • BSc/HBO (or equivalent) in Biochemistry, Biology, Pharmaceutical degree or relevant education.
  • Ability to drive collaboration in a fast-paced environment
  • Around 2 years of QA experience in the biotechnological/pharmaceutical or related industry
  • Knowledge and Experience in vaccines is a plus
  • Experience with documentation systems like Trackwise, True Vault is preferable
  • Experience in Change control and all documenting related activities is a plus
  • Problem-solving and analytical capability, eye for details
  • Good communicative and advisory skills in English both in word and writing. Dutch is a plus
  • Able to work independently as well as in a team

 

If you meet our requirements and are interested in hearing more about our Quality Assurance Officer role, please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!


 

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