Quality Assurance Associate

2-7-2020 kampenhout
description de la société

IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux. Their offices are located at “Hof ter Loonst” in Kampenhout. Since they are expanding their team we are looking for an experienced Quality Assurance Associate who has the ambition and potential to grow in their organization. All projects within IN2Pharma are worked on in close cooperation with one or more colleagues and for some projects, you also work on site at the clients’ offices for 1 or 2 days per week.

Interested? Apply by sending me your resume and cover letter to laurence.teerlynck@cx.ausy.be or call me on 03 369 19 80.

description de la fonction

Are you an experienced Quality Assurance Associate who has the ambition and potential to grow in a motivating organization? Then we are looking for you!

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
  • Draft, implement and monitor quality agreements
  • 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

vos atouts

What do you need to be successful?

  • Level of education: Master degree in life sciences
  • Experience within Quality Assurance: GDP, Quality Management System, Quality Control
  • Familiar with good documentation practices and project management
  • Good communication skills in Dutch, French, English (both written and verbal)
  • Proficient with computer and Microsoft Office
  • 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 client offers you:

  • 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

spécialiste en qualité et environnement (m/f)
type de job
temps plein
type contrat
jobs fixes immédiat
informations de contact
Laurence Teerlynck
laurence.teerlynck@cx.ausy.be 03 369 19 80
03 369 19 80