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Quality Assurance Project Manager – Maastricht / Geleen


The company

Our client is a global organization, focused on achieving the strategic vision of being the world’s leading, integrated solutions provider in pharma and consumer healthcare and nutrition customers all along the healthcare continuum. The company has more than 100 sites and offices and approximately 14,500 full-time employees worldwide. We are looking for a Quality Assurance Project Manager to work at one of the company’s sites located in the south of Limburg Province, the Netherlands.


The Quality Assurance (QA) Project Manager is assigned as the primary liaison to an external customer(s) for all quality-related items including temporary and permanent change controls, deviations, standalone investigations, CAPAs, Product Quality Reviews and Quality Agreements and facilitates discussions between customers and internal groups such as MSAT (Manufacture, Science and Technology), Manufacturing, Engineering and QC (Quality Control).

For these quality-related items, the incumbent manages the process for notifying the customer and assuring the customer’s feedback and comments are addressed, verifies that the quality records are complete; that there is sound justification/scientific rationale, that root cause analysis and corrective and preventive action is appropriate and, where applicable, that customer approval is received.

The QA Project Manager leads Joint Quality Team meetings –establishes agendas, publishes meeting minutes and tracks action items; participates in Internal and Joint Project Team (IPT/JPT) meetings as the QA representative and tracks and publishes monthly and quarterly quality KPIs.

The QA Project Manager makes quality decisions and performs problem-solving however high risk items such as major or critical deviations, change controls and CAPA will require input and agreement from the department manager.

Key responsibilities:

  • Partner with internal functional areas as part of the change control process.
  • Support the Deviation, Investigation, and CAPA processes specific to their assigned customers;
  • Review and approve investigation reports including root cause analysis and assure corrective and preventive actions address the root cause to prevent recurrence
  • Interact with internal and external customer as part of Joint and Internal project Teams serving as the Quality Subject Matter Expert for any customer related quality issues.
  • Track and present customer metrics.
  • Review and approve various product specific documents such as Quality Agreements, Product Quality Reviews etc.
  • Support customer audits.


  • Bachelor’s Degree or equivalent experience. Preferred area of study: Scientific related field
  • 3-7 or more years in GMP environment. Minimum 3-5 years in Quality Assurance or similar discipline. Biotechnology manufacturing background is preferred
  • Knowledge of GMP’s and regulations
  • Project Management Experience: Presentation, Customer Liaison, Meeting facilitation
  • Experience with Trackwise, SAP, Document management system preferred
  • Detail-oriented
  • Organized
  • Self-motivated
  • Displays a clear willingness to listen to others
  • Demonstrates quality decision making
  • Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused, works well under pressure, capable of making quality decisions. Practices safety awareness at all times.


What do we offer?

  • A high tech work environment.
  • Career growth possibilities.
  • Very good comansation package
  • Modern secondary conditions of employment (pension scheme, 8% holiday allowance, end-of-year bonus).

If you do not already live in the south of Limburg region, you have to be willing to relocate. Depending on your circumstances, you will be eligible for an allowance to help cover your moving costs.


Please contact Robin Bisschoff (+31 6 14 79 56 47) if you have any questions about this position.


Please apply via the “Apply” button. We are looking forward to receiving your application!

By |October 2nd, 2019|Laboratorium, Vacancies|0 Comments

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