Senior Medical Devices Auditor
79% Flex
Offer summary
Qualifications: Minimum Bachelor's Degree in Science or Engineering, 10 years' experience in Medical Devices Manufacturing/Industry with 3 years in quality or regulatory functions, 5 years auditing experience for ISO 13485, MDSAP, MDD, IVD, IVDR, UKCA, and MDR standards, RAB/QSA or IRCA approved Quality auditing training completion required, Registered Quality Lead Auditor with strong regulatory and FDA 510(k) experience.
Key responsabilities:
- Perform third party audits and technical information review using SGS Certification procedures and ISO standards
- Lead audit teams, collect, and analyze data to recommend certification
- Conduct audits to ensure manufacturers comply with relevant standards and regulations
- Provide technical advice, presentations, and maintain professional communication with clients
Job description
Required profile
Experience
Level of experience :
Expert & Leadership (>10 years)Industry :
Spoken language(s)
Check out the description to know which languages are mandatory.
Soft Skills
- Team player
- Excellent communication and presentation skills
- Analytical thinking
- Strong leadership capabilities
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