Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.

Job Information

Zimmer Biomet Supplier Quality Assurance Lead Auditor (ISO 13485:2016) in Remote, United Kingdom

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered, and recognized.

What You Can Expect

This GBS position is responsible for timely planning and completion of supplier audits for the EMEA region. The role involves interaction with internal and external stakeholders to ensure supplier audits are scheduled and completed on time, including required follow ups and resource assignment. This position requires strong understanding of medical device industry requirements and significant auditing experience ( ISO 13485:2016 Lead auditor qualification – required).

How You'll Create Impact

  • Creation and maintenance of the supplier audit schedule for the EMEA region.

  • Planning and conducting the audits in line with the defined requirements.

  • Compiling supplier audit reports within set timeline.

  • Facilitate training of newly trained auditors.

  • Compiling Supplier documentation required based on the qualification type and supplier risk category.

  • Coordination of SCARs raised from supplier audits.

  • Provide input into the metrics review meeting, ensuring any issues related to supplier audits are raised and addressed.

  • Preparation of supplier performance monitoring data required to fulfill the supplier qualification requirements.

  • Maintenance of supplier ISO certificates in the electronic system.

  • Support site supplier quality teams with PMML, SCNs and DRMs.

What Makes You Stand Out

  • English language skills (fluency in reading, writing, listening, and speaking).

  • Strong writing and communication skills.

  • High level of accuracy

  • Responsible, professional, detail oriented.

  • Strong computer skills.

Your Background

  • Bachelor’s Degree in life sciences, technical (engineering), medical sciences – required

  • Experience of working within medical device environment (minimum 2 years) – required

  • Significant auditing experience – required

  • Supplier audit experience - required

  • ISO 13485:2016 Lead auditor qualification – required

  • Understanding of MDR requirements – required

  • Understanding of other ISO standards including ISO/IEC 17025 and ISO 11135 - preferred.

Travel Expectations

  • Up to 30%

EOE/M/F/Vet/Disability

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