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Salary
≈ $53k – $90k per year (Estimated)
Location
In office (Leiden)
Seniority
Senior · 7+ years exp
Employment
Contractor

First seen by Alion on Jun 4, 2026. SIRE Life Sciences scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Headquartered in Leiden, Netherlands, SIRE Life Sciences is a specialized recruitment, executive search, and talent management consultancy dedicated exclusively to the European life sciences sector. The enterprise provides a broad range of human capital solutions, including permanent recruitment, interim contracting, secondment, and executive search for the pharmaceutical, biotechnology, medical device, and healthcare industries. By combining deep domain specialization with technology- and data-driven recruitment methodologies, it connects highly skilled scientific, technical, and executive talent with Life Sciences organizations across Europe.
The Company

Our client is a global healthcare and life sciences organization with a strong presence in the Netherlands, focused on developing innovative therapies and vaccines to address major global health challenges. The company operates in a highly regulated, technology-driven environment and promotes a collaborative culture centered on innovation, quality, and continuous improvement.

About the Role:

This role is focused on leading quality investigations within a pharmaceutical manufacturing environment, ensuring product quality, compliance, and operational excellence. The Senior Quality Engineer manages non-conformance investigations, CAPA activities, and change controls while identifying root causes and implementing corrective actions. The position collaborates closely with cross-functional teams to maintain regulatory compliance, improve processes, and ensure timely closure of quality records.

Responsibilities:

- Lead and manage quality investigations, including non-conformances, root cause analysis, and resolution of quality issues.

- Oversee CAPA and Change Control processes to ensure timely implementation of corrective and preventive actions.

- Review and maintain quality documentation, ensuring compliance with GMP, regulatory requirements, and internal standards.

- Conduct risk assessments, implement mitigation plans, and drive continuous quality improvement initiatives.

- Coordinate cross-functional teams, monitor investigation progress, and communicate risks, findings, and outcomes to stakeholders and management.

Requirements:

- Relevant Bachelor's (HBO) degree with 7-10 years of experience in Quality Engineering, investigations, or pharmaceutical manufacturing.

- Strong experience managing non-conformance investigations, CAPA activities, and Change Control processes within a GMP-regulated environment.

- Proven expertise in root cause analysis, risk assessment, problem-solving, and continuous improvement methodologies.

- Excellent stakeholder management, communication, and cross-functional team coordination skills with the ability to manage multiple priorities.

- Proficiency in MS Office, data analysis, and quality systems, combined with strong organizational skills and English language proficiency (B2+).

Other Information:

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