DNV Business Assurance USA Inc. seeks a Senior Lead Auditor - Medical Devices to work for our office in Houston TX.
Job Duties:
Opportunities Beyond Business
Our mission is to safeguard life property and the environment. By joining us you will work towards our meaningful vision to make a global impact for a safe and sustainable future. DNV offers a congenial working environment competitive salaries and an exceptional benefits package.
Local employment conditions apply.
Company & Business Area Description
DNV is one of the worlds leading certification bodies. We help businesses assure the performance of their organizations products people facilities and supply chains through certification verification assessment and training services. Partnering with our customers we build sustainable business performance and create stakeholder trust across all types of industries.
Equal Opportunity Statement
DNV is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without regard to gender religion race national or ethnic origin cultural background social group disability sexual orientation gender identity marital status age or political opinion. Diversity is fundamental to our culture and we invite you to be part of this diversity! For more information about your rights under the law see: Requirements:
In lieu of a Bachelors degree in above stated fields and four (4) years of above stated experience employer will accept a Masters degree in Biology or Microbiology Chemistry or Biochemistry Computer and Software Technology Electrical Electronic Mechanical engineering or Bioengineering Human Physiology Medicine or Veterinary Medicine Pharmacy Physics or Biophysics Food Science or related field of study and two (2) years of experience as a Medical Device Auditor Lead Auditor or related role where required experience gained.
Special Skills: Also requires experience in the following:
Entire process of auditing medical device quality management systems including documentation review risk management of applicable medical devices implementation audit and audit reporting with an accredited CB/NB;
Participated as a trainee in a minimum of four audits totaling at least 20 days in an accredited QMS program with at least 50% of that time against ISO 13485 in an accredited program;
Acting in a team leader role under the supervision of a qualified team leader for at least three ISO 13485 audits;
ISO 13485:2016 36-40 Hour lead auditor certification;
20 audit days in ISO 9001/ISO 13485 or combination of both as a 3rd party lead auditor;
MDR Training;
MDSAP Training; and
ISO 14971:2019 Training.
Driven by our purpose of safeguarding life, property and the environment, DNV enables organizations to advance the safety and sustainability of their business.