Quality Director

Posted Yesterday
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Bloomington, MN, USA
In-Office
Senior level
Healthtech • Manufacturing
The Role
Leads quality control and quality assurance activities for a medical device distribution site, including receiving inspection, product release, supplier and contract manufacturing quality, nonconformances, audits, inspection readiness, and quality improvement. Oversees regulatory compliance, returned product analysis, FDA reporting, supplier change assessments, and product distribution quality. Provides direct leadership to quality inspectors, technicians, specialists, and engineers while partnering with cross-functional and global teams.
Summary Generated by Built In

Saluda Medical is a commercial‑stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed‑loop neuromodulation platform. The company’s proprietary technology senses and measures neural responses to stimulation and automatically adjusts therapy based on real‑time neurophysiological feedback.

Saluda Medical’s first product, the Evoke® System, is designed to deliver known, consistent, and personalized spinal cord stimulation therapy by objectively measuring neural responses and maintaining therapy within a prescribed therapeutic window. Saluda Medical is headquartered in Minneapolis, Minnesota.

At Saluda, we challenge boundaries. We innovate and think beyond the conventional. Our focus is to revolutionize the standard of care in neuromodulation to positively impact patient’s lives.

The Quality Director reports to the VP QA and is responsible for managing the company’s quality activities at the Bloomington, Minnesota site.

What You’ll Do:

  • Manage all quality control (QC) activities, to include receiving inspection and product release from the site.
  • Manage all quality assurance activities in the distribution facility, to include non-conformance reports (NCR) and supplier quality for our contract manufactured and OEM acquired products.
  • Ensure activities performed in the facility are compliant to global regulatory requirements for which we claim compliance, as well as Saluda business expectations.
  • In partnership with the head of US Distribution and Customer Service, be a vocal advocate for a strong culture of quality and compliance at the site.
  • Build strong working relationships with other cross-functional leadership at the site to include Supply Chain, Distribution & Customer Service, Clinical, Sustaining Engineering, and Regulatory Affairs.
  • In partnership with the head of US Distribution and Customer Service, ensure products distributed from the facility are handled appropriately and distributed to customers accurately and in a timely manner.
  • Provide direct leadership to inspectors, technicians, quality specialists and engineers utilizing an inclusive and empowering leadership approach.
  • Manage distribution, contract manufacturing and OEM-related quality challenges as they arise.
  • Develop and ensure the implementation of a site inspection readiness plan.
  • Participate internal and external audits to ensure the site’s quality system is effective.
  • Manage and lead quality improvement projects in all areas of responsibility.
  • Organize Supplier Change Assessment Board meetings and ensure submitted change request has the required information for the Change Assessment Board.

What You’ll Bring:

  • Bachelor of Science degree or higher in a life sciences or engineering discipline  
  • At least 5+ years of experience in medical device quality with 2+ years of leadership experience.
  • Proven ability to execute and maintain quality systems, with direct experience in post-market quality, distribution quality, or supplier quality.
  • Strong relationship builder and communicator with diverse work teams
  • Experience building strong relationships with global colleagues.
  • Ability to work on-site 4+ days a week.
  • Prior experience with returned product analysis and oversight of U.S.
  • FDA 21 CFR Part 806 reporting obligations.

Our Core Values:

  • People – Our first responsibility is to the patients we serve.
  • Integrity – Do the right thing
  • Pioneering – Lead Boldly, Change Lives, Disrupt the Status-Quo
  • Performance – Win together – Deliver with Excellence.

Saluda Medical embraces diversity and equal opportunity. We are committed to building a team representative of a variety of backgrounds, perspectives and skills. We believe people are the source of our inspiration and innovation.

Saluda Medical does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Saluda Medical’s approved agency list. Unsolicited resumes or candidate information submitted to Saluda Medical by search/recruiting agencies not already on Saluda Medical’s approved agency list shall become the property of Saluda Medical.

Skills Required

  • Bachelor of Science degree or higher in a life sciences or engineering discipline
  • At least 5 years of experience in medical device quality
  • At least 2 years of leadership experience
  • Experience executing and maintaining quality systems
  • Direct experience in post-market quality, distribution quality, or supplier quality
  • Strong relationship-building and communication skills with diverse work teams
  • Experience building relationships with global colleagues
  • Ability to work on-site at least 4 days per week
  • Experience with returned product analysis
  • Experience overseeing U.S. FDA 21 CFR Part 806 reporting obligations
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The Company
HQ: Sydney
482 Employees
Year Founded: 2011

What We Do

Saluda Medical is a global company revolutionizing the field of neuromodulation with an emerging portfolio of therapies driven by advanced closed-loop technologies designed to treat debilitating neurological disorders. The company’s first product, the Evoke® System, is the only ECAP-controlled closed-loop spinal cord stimulation (SCS) system and is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with failed back surgery syndrome, intractable low back pain, and leg pain. The Evoke System instantaneously reads, records, and responds to the nerves’ response to stimulation to provide continually optimized therapy and is proven to be superior to open-loop SCS for the treatment of overall trunk and/or limb pain. 12-month results from the EVOKE Study, the first double-blind randomized controlled trial (RCT) used in support of Premarket Approval (PMA) in spinal cord stimulation history, were published in The Lancet Neurology and 24-month results have since been published JAMA Neurology. Both studies are poised to set new clinical standards for long-term pain relief and improvements in physical and emotional functioning, sleep quality and health-related quality of life. In the EU, Evoke is CE Marked and commercially available. In the U.S., Evoke is FDA-approved and will be available when the Company implements its full commercial release in 2023. Saluda Medical is a privately held company with headquarters in Bloomington, MN, USA. To learn more about Saluda Medical, including the risks & important safety information, visit www.saludamedical.com

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