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Saluda Medical

ECAP-guided spinal cord stimulation therapy

Quality Director

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBloomington, MN, USANo salary listed

About the Job

Requirements

  • A Bachelor of Science degree or higher in a life sciences or engineering discipline.
  • At least 5 years of experience in medical device quality, including 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.
  • Experience building strong relationships with global colleagues.
  • Ability to work on-site at least 4 days a week.
  • Prior experience with returned product analysis and oversight of U.S. FDA 21 CFR Part 806 reporting obligations.

Responsibilities

  • Manage all quality control activities, including receiving inspection and product release from the site.
  • Manage all quality assurance activities in the distribution facility, including non-conformance reports and supplier quality for contract-manufactured and OEM-acquired products.
  • Ensure facility activities comply with global regulatory requirements for which the company claims compliance, as well as company business expectations.
  • Partner with the head of U.S. Distribution and Customer Service to advocate for a strong culture of quality and compliance at the site.
  • Build working relationships with cross-functional leadership at the site, including Supply Chain, Distribution and Customer Service, Clinical, Sustaining Engineering, and Regulatory Affairs.
  • Partner with the head of U.S. Distribution and Customer Service to ensure products distributed from the facility are handled appropriately and delivered to customers accurately and promptly.
  • Provide direct leadership to inspectors, technicians, quality specialists, and engineers using an inclusive and empowering leadership approach.
  • Manage distribution, contract manufacturing, and OEM-related quality challenges as they arise.
  • Develop and ensure implementation of a site inspection readiness plan.
  • Participate in 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 requests contain the required information for the board.

About the Company

Saluda Medical

ECAP-guided spinal cord stimulation therapy

Saluda Medical develops neuromodulation therapies for chronic pain by focusing on spinal cord stimulation. Its Evoke System uses Evoked Compound Action Potentials to measure the spinal cord’s response to stimulation and adjusts parameters in real time for each patient. This closed-loop approach relies on objective neural signals rather than fixed settings, aiming for consistent pain relief and personalized therapy, supported by clinical trial data. The company seeks to broaden neuromodulation use by providing precise, measurable neural activation readouts to clinicians.

Company size
501-1,000
Company stage
IPO
Headquarters
Sydney NSW, Australia
Founded
2013

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