Quality Assurance Officer (0.6 FTE)


As Quality Assurance (QA) Officer you give effect to InnoCore’s quality policy and quality system. In close collaboration with the Quality Assurance Manager, you maintain and improve the quality system and procedures. Your responsibilities include (but are not limited to) document management and document control, including document review and approval, issuance and archiving. You report to the Quality Assurance Manager.

 

As a QA Officer you:

  • Manage and perform document control activities
  • Perform administrative tasks related to the quality system
  • Review and approve master work instructions, logbooks, and registration forms
  • Review and approve filled in logbooks, calibrations, analysis records, and operational records
  • Perform internal audits
  • Support the QA manager during customer audits and regulatory inspections
  • Support the QA manager for the QA release of products intended for non-clinical safety studies (GLP Toxicology) and products intended for human use (GMP)
  • Stimulate quality awareness throughout the organization

 

Profile and background

In addition to a MBO+ or HBO degree in life sciences and/or chemistry, and at least 3 years’ experience in a pharmaceutical company (preferably in Quality Assurance), you:

 

  • Have a broad knowledge – gained through at least 3 years of relevant experience - of quality systems in the pharmaceutical industry
  • Embrace teamwork and cross-functional collaboration
  • Take ownership and are self-organized
  • Are eager to do things first time right with a strong customer focus and strong insight in quality factors in order to find the best practical solution fulfilling the appropriate quality requirements
  • Have a quality mind-set and hands-on mentality
  • Are self-aware, self-critical and open to receive/give feedback in a respectful and transparent way
  • Are eager to grow by challenging your own limits of knowledge and experience
  • Have strong affinity with quality at work and strong awareness of company procedures and GMP/GLP guidelines
  • Can effectively transfer knowledge to others. You have good reporting and verbal communication skills and are proficient in English
  • Show a strong ‘I care mentality’ by taking on responsibility and showing accountability for HSE risks towards yourself, colleagues and third parties

 

Offer

We offer a challenging position in a modern and well equipped laboratory where you will become part of a young and ambitious team of co-workers. Remuneration will be according to standards in the pharmaceutical industry. At InnoCore we are committed to offer the best possible environment for our employees, where people are challenged and supported to further develop themselves. We believe in providing a collaborative, creative environment where each member of the team feels encouraged to contribute to our processes, decisions, planning, and culture.

 

Further information and how to apply

For more information please contact Marco Lutz (QA Manager) at +31 (0)50 575 3100. You can email your curriculum vitae and motivation letter to jobs@innocorepharma.com

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