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Contract Opportunity - Medical Device Auditors

Role overview

Qualifications

  • 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 ISO 13485, MDSAP, MDD and MDR
  • Strong background and knowledge of technical applications of the standards

Responsibilities

  • 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

Key facts

Other skills

  • Decision Making
  • Communication
  • Social Skills
  • Organizational Skills
  • Problem Solving

About the company

SGS  logo

SGS

Audit & Assurance Services

We are SGS – the world’s leading testing, inspection and certification company. We are recognized as the global benchmark for quality and integrity. Our 96,000 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Community Guidelines Welcome to our LinkedIn page! SGS encourages all fans of this page to participate in the conversation through questions and comments. Any comments or activity arising from persons sharing or otherwise reproducing any communications published by SGS is not controlled or endorsed by SGS. We want to promote an informative and enjoyable environment within this community; we therefore ask that you post content that is both relevant and respectful and that you follow LinkedIn's Professional Community Guidelines; https://help.linkedin.com/app/answers/detail/a_id/34593/~/linkedin-professional-community-guidelines Posts will be removed if they are: - Offensive, defamatory, discriminatory or obscene - Fraudulent, deceptive or misleading - In violation of any intellectual property rights - In violation of any law or regulation - Abusive, harassing, stalking, threatening or attacking others - Trolling or deliberate disruption of discussion - Commercial solicitations or personal promotion - Spam, link baiting or files containing viruses that could damage the operation of other people’s computers or mobile devices

Company details

Company typeLarge
IndustryAudit & Assurance Services
Company size10001

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Job description

Company Description

SGS is the world’s leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 96,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world.

Job Description

We are looking for Contract Medical Device Auditors with:

  • 2+ years of direct Sterilization (primarily EO and Gamma) experience (required)
  • experience with cardiovascular soft tissue implants (MDN1101) and/or general non-active non-implantable devices used in healthcare and others non-actives non-implantable devices (MDN1214) (preferred)
  • experience with ISO 14001, ISO 45001 and/or ISO 50001 based management systems (preferred)

As a Contract Medical Device Auditor, you will perform third-party audits per SGS Certification procedures and the requirements for standards such as ISO 13485, MDSAP, MDD and MDR. You will be responsible for making relevant decisions concerning the audit process and to inform SGS as required to resolve issues outside the audit process. The Contract Medical Device Auditor is responsible for collecting and analyzing 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.
  • Adheres to internal standards, policies, and procedures

Qualifications

Education and Experience

  • Bachelor’s degree in a related discipline (i.e., Engineering, Bioscience, Biomedical, Science, etc.) AND
  • 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

Knowledge/ Skills/ Abilities

  • Preferred Experience with:
  • Non-active cardiovascular, vascular, and neurovascular implants
  • Non-active, non-implantable ophthalmologic devices
  • Sterilization experts (ETO, Irradiation, Moist Heat)
  • ISO 9001 qualification
  • Strong background and knowledge of technical applications of the standards
  • Language Skills: Highest advanced level of English
  • 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
  • Computer Skills
  • MS Office Suite (Word, Excel, PowerPoint) – Intermediate user proficiency

Travel

  • Travels up to 80% of the time (automobile & airplane).  
  • Must be able to travel to Canada and Mexico to perform audits
  • Weekend travel may be necessary to meet scheduling requirements.

Additional Information

SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.

This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.

If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back.  Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

All your information will be kept confidential according to EEO guidelines.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
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