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SGS

Contract Opportunity - Medical Device Auditors

RemoteUnited States, Canada, Mexico only
Published
Experience
Mid
Employment
Contract
Company size
Enterprise
Salary not disclosed
Check eligibility

Open to US, CA, MX only. Set where you work from to check your eligibility.

No BS summary

Contract medical device auditor authorized to travel and provide auditing services in the United States, Canada and Mexico. Needs 4+ years with medical devices under ISO 13485, MDSAP, MDD and/or MDR compliant QMS, ISO 9001 qualification, advanced English, and up to 80% travel.

Core skills

ISO 13485MDSAPMDR

Required skills

MDDISO 9001MS Office

Optional skills

ISO 14001ISO 45001ISO 50001GMP

Required languages

English Highest advanced level of English

Optional languages

Spanish preferred

What you'll do

  • Perform third-party audits per SGS Certification procedures and the requirements for standards such as ISO 13485, MDSAP, MDD and MDR.
  • Make relevant decisions concerning the audit process and inform SGS as required to resolve issues outside the audit process.
  • Collect and analyze sufficient information to provide a recommendation for certification.
  • Perform audits for clients’ medical device quality systems and technical information to the requirements of ISO 13485 and other regulatory requirements such as MDSAP, MDD, MDR and EU.
  • Decide upon evidence gained during audits whether or not registration should be recommended or allowed to continue.
  • Participate actively in witness audits by SGS or accreditation bodies.
  • Maintain all audit credentials.
  • Adhere to internal standards, policies, and procedures.

What they require

  • Must be authorized to travel to and provide auditing services in the United States, Canada and Mexico.
  • Non-active cardiovascular, vascular, and neurovascular implants (2+ years).
  • Non-active, non-implantable ophthalmologic devices (2+ years).
  • General non-active non-implantable devices used in healthcare and others non-actives non-implantable devices (2+ years).
  • Sterilization experts, primarily EtO, Irradiation and Moist Heat, as well as other sterilization technologies.
  • ISO 9001 qualification.
  • Bachelor’s degree in a related discipline, i.e., Engineering, Bioscience, Biomedical, Science, etc.
  • Minimum 4 years of experience working with medical devices under ISO 13485, MDSAP, MDD and/or MDR compliant QMS.
  • Preferred: Possesses Auditor Credentials for one or more of these standards: ISO 13485, MDSAP, MDD and MDR.
  • Preferred: GMP pharmaceutical, cosmetics, dietary supplements, etc. quality / regulatory experience.
  • Non-active cardiovascular, vascular, and neurovascular implants (MDN1101).
  • Non-active, non-implantable ophthalmologic devices (MDN1206).
  • General non-active non-implantable devices used in healthcare and others non-actives non-implantable devices (MDN1214).
  • Sterilization technologies, primarily EtO, Irradiation and Moist Heat; other technologies are also considered.
  • Strong background and knowledge of technical applications of the standards.
  • Excellent communication and interpersonal, verbal, written and presentation skills.
  • Proactive attitude and excellent organizational skills.
  • Effectively reacts in stressful situations and makes clear, well-founded decisions regarding conformity during the audit.
  • Ability to multitask and manage multiple projects while delivering results on time.
  • Act with integrity, tact and character.
  • MS Office Suite (Word, Excel, PowerPoint) – Intermediate user proficiency.
  • Travels up to 80% of the time by automobile and airplane.
  • Weekend travel may be necessary to meet scheduling requirements.

SGS

SGS is the world’s leading testing, inspection and certification company, recognized as the global benchmark for sustainability, quality and integrity. It operates laboratories and business facilities across 115 countries.

🇨🇭 SwitzerlandTestingEnterprisesgs.com
Salary not disclosed