Senior GMP Quality Engineer
SIRE® Life Sciences
Senior GMP Quality Engineer
Samenvatting
Wat krijg je?
Wat ga je doen?
- Lead and manage quality investigations
- Oversee CAPA and Change Control
- Review and maintain quality documentation
- Conduct risk assessments and mitigations
- Communicate risks and findings to stakeholders
Wat verwachten wij?
- 7 tot 10 jaar ervaring in Quality Engineering
- Ervaring met non-conformances en CAPA in GMP-omgeving
- Expertise in root cause analysis en risicoanalyse
- Ervaring met MS Office en kwaliteitssystemen
Volledige vacaturetekst
Our client is a global healthcare leader focused on developing innovative therapies and vaccines to solve global health challenges. As a Senior Quality Engineer, you will lead complex investigations and root cause analyses within a high-tech GMP environment. You will collaborate with cross-functional teams to drive innovation and quality improvements. Ready to impact global health? Take the lead in this technology-driven culture and apply today!
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:
Looking for a new opportunity? Well, it's right here! If you're interested, please click the below button to apply for the job.
58148
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