Validation Engineer
9-12 Month Contract with potential extension
4+ Days On-Site
Baden-Württemberg
What You'll Do
- Maintain and continuously improve the Quality Management System (QMS)
- Manage CAPAs, non-conformances and change controls
- Lead and support Root Cause Analysis (RCA) and investigations
- Support internal, external and regulatory audits
- Review and maintain SOPs and quality documentation
- Monitor quality metrics and identify continuous improvement opportunities
- Support document control, training and compliance activities
- Partner with Quality, Regulatory, Engineering and Operations teams
What We're Looking For
- A minimum of 2-3 years of quality experience within medical devices or another highly regulated industry
- Strong knowledge of ISO 13485 and Quality Management Systems
- Hands-on experience with CAPA, RCA, non-conformances and audits
- Knowledge of EU MDR, FDA QMSR and/or MDSAP advantageous
- Strong communication, problem-solving and stakeholder management skills
FAQs
Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your resume and details on file so when we see similar roles or see skillsets that drive growth in organizations, we will always reach out to discuss opportunities.
Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.
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That's why we recommend registering your resume so you can be considered for roles that have yet to be created.
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