The Company
We are a leading global organization in the life sciences and health technology sector, committed to advancing healthcare through high-quality products and innovative solutions. The company values compliance, quality, and continuous improvement, ensuring safety and excellence in every aspect of its operations.
Role Description
We are seeking a Quality Assurance Specialist to conduct comprehensive audits of processes, systems, documentation, and facilities to ensure adherence to internal procedures, industry standards, and global regulatory requirements. The role involves reviewing production and analytical documentation, identifying compliance gaps, and collaborating with cross-functional teams to implement corrective actions. The successful candidate will combine technical expertise, regulatory knowledge, and strong analytical skills to maintain the highest quality standards across operations.
Key Responsibilities
- Conduct routine audits of data, processes, systems, equipment, and facilities to ensure compliance with SOPs, GMPs, and regulatory standards.
- Review and approve production and analytical documentation supporting the release of products, ensuring conformance to regulatory requirements.
- Identify audit findings, communicate results effectively, and work with teams to implement corrective and preventive actions.
- Prepare clear audit reports summarizing deficiencies and recommendations for improvement.
- Collaborate with cross-functional stakeholders including production, quality, and regulatory teams to support compliance initiatives.
- Participate in risk assessments and support continuous improvement of audit processes.
- Maintain up-to-date knowledge of regulatory guidelines and industry best practices.
Requirements
- Minimum 2 years of experience in a pharmaceutical or GMP-regulated environment.
- Proficiency in Dutch (must-have).
- Practical experience with deviation management, change management, and event handling.
- Previous experience in a specialist or QP-related role (without formal QP responsibility).
- Strong communication skills and ability to work independently.
- Affinity for complex quality issues and project-based work.
- Living within reasonable travel distance to Boxmeer (preferred).
Other Information
If you are a proactive professional with a keen eye for detail and a passion for maintaining high-quality standards, this opportunity is for you. Apply now to contribute to a culture of excellence and regulatory compliance.
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About us
Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.
SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.
Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.
Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.