We are looking to expand our team with a Quality Assurance Associate who has the ambition and potential to grow in our organization. You will be integrated in the QA team and for some projects, you also work on site at the clients’ offices for 1 or 2 days per week.

Main Areas of Responsibility

As a QA Associate, you will support the RP in setting up, improving and maintaining quality standards for pharmaceutical and healthcare companies in Benelux.

  • Establish and maintain a quality system: SOP management, change control, training, CAPAs, etc
  • Review packaging specifications and technical changes in preparation of administrative batch release
  • Coordinate and investigate product quality complaints and non-conformances
  • Perform self-inspections and assist in external audits
  • Interact with regulatory department, suppliers and contract manufacturing organizations
  • Cooperate with the QA department of the clients’ other EU affiliates
  • Participate in quality related audits or inspections from health authorities
  • Stay up-to-date with the latest developments and relevant legislation

Technical Skill Requirements

  • Level of education: Master degree in life sciences
  • Experience within Quality Assurance: GDP, GMP or ISO
  • Good communication skills in Dutch, French, English (both written and verbal)
  • Proficient with computer and Microsoft Office

Competencies that are an asset

  • Strong initiative, pragmatic and problem solver
  • Technical knowledge of GMP, regulatory affairs
  • Detail oriented: concern for quality, compliance and consistency
  • Good communicator & team player

Our offer

  • A permanent full-time position with a competitive package and supplementary benefits
  • Motivating work environment at an exclusive location
  • Personal development plan and development opportunities by working closely together on challenging projects in different situations and for several pharmaceutical companies

 


Interested ?   
Send your CV and motivation to jobs@in2pharma.com

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