Job Description

Company DescriptionWe are SGS - the world\'s leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.This position performs third party audits in Canada and the US and technical information review per SGS Certification procedures and the requirements of ISO 9001, ISO 13485, ISO 13485 under CMDCAS, MDD, MDSAP, IVDR, UKCA and/or JPAL.

• Lead Auditors have authority for the control and performance of auditing activities including planning and the control of other members of audit teams.
• Lead a team of auditors in performing medical device audits, in conformance with the SGS Global/Local procedures
• This position is responsible to collect and analyze sufficient information to provide a recommendation for certification.
• Access and review North American clients\' medical devices quality systems and technical information to the requirements of ISO 9001, ISO 13485 and other regulatory requirements for access into Canada, EU, and Japan. Review technical dossiers to the requirements of 93/42/EEC (MDD) and/or 98/79/EC (IVDD).
• Decide upon evidence gained during audits whether or not manufacturers are in compliance with all relevant standards / regulations, and if registration should be recommended or allowed to continue.
• Provide technical advice to marketing and sales functions, as required. Utilize and maintain professional communication and presentation skills while meeting with clients.
• Conduct public presentations / seminars on specific standards, where required.

Qualifications

• Education: Minimum Bachelor\'s Degree in Science or Engineering, or equivalent
• 10 years\' experience in Medical Devices Manufacturing/Industry with 3 years minimum experiences in quality or regulatory related functions.
• Minimum 5 years of experience auditing for ISO 13485, MDSAP, MDD, IVD, IVDR, UKCA, and MDR standards.
• Satisfactory completion of an RAB/QSA or IRCA approved training course in Quality auditing. The course(s) must include an examination, which must be passed to evidence satisfactory completion.
• Registered (IRCA and/or RAB/QSA) Quality Lead Auditor is a MUST
• Strong background in either design engineering or research and development
• Global Regulatory Affairs background, including MDD / IVDD.
• FDA 510(k) experience
• Experience in radiation, neurological, soft tissue implant, absorbable products, orthopedic, active therapeutic/diagnostic supplying energy, active administration, animal tissue, and/or combination product devices
• Have competent working knowledge of nationally recognized Quality Management System auditing standards and procedures.
• Broad knowledge of engineering and technical applications used in the development of medical devices.
• Ability to travel (80% -100%) to the US, including a valid driver\'s license.
• Extended hours and shift work may be required from time to time.

Additional InformationSGS Canada is an equal opportunity employer and we are committed to achieving greater accessibility by providing accommodation for people with disabilities during our hiring process. Accommodations are available on request for qualified candidates during each stage of the recruitment process.We are prepared to receive applications from candidates not based in Canada and can support visa and relocation fees.#SGSSJ

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