Coordinate quality systems, audits and follow-up actions in a pharmaceutical environment. This senior QA role in Geleen requires at least five years of relevant experience and good spoken and written Dutch and English.
The role
As Senior QA Officer at our client company in Geleen, you will work in a pharmaceutical environment and coordinate the implementation and maintenance of quality management systems. The focus is mainly on GMP/GDP, with some involvement in ISO 13485/MDR.
Key responsibilities
- Facilitate the introduction of new GMP, GDP and MDR requirements.
- Monitor training compliance and deliver GDP/GMP training to employees and management.
- Conduct internal and external GMP/GDP audits and oversee follow-up actions. You will also support GMP/GDP audits and inspections by authorities and customers.
- Help establish work processes and ensure their effectiveness and efficiency.
- Oversee the documentation of these activities, ensuring that documented evidence is complete and traceable.
- Contribute to management reviews, support supplier qualification, and review and draft Product Quality Reviews (PQRs).
- Track and report quality complaints, deviations, changes and CAPAs.
What you bring
- HBO-level working and thinking ability (the Dutch higher professional education level).
- At least five years of relevant experience; experience in a GMP and/or GDP environment is preferred.
- Accuracy, resilience under pressure, willingness to learn, strong communication skills and a collaborative approach across disciplines.
- Persuasive and analytical skills.
- Good spoken and written Dutch and English.
- An affinity with software systems.
What is offered
- A challenging, responsible position in a dynamic, growing organization.
- A competitive salary and benefits, including flexible working hours, hybrid working, 28 days off and a pension.
- Opportunities for professional development and growth.
- An inspiring, collegial working environment with an international character.