Position Profile:
Saluda is a global healthcare company that is redefining Spinal Cord Stimulation (SCS) therapy at the intersection of automated algorithms, real-time diagnostics, and ground-breaking clinical evidence. The Saluda difference is defined by Dose-Control Technology via measurement of physiological response.
At Saluda, we challenge boundaries. We innovate and think beyond the conventional. We disrupt. With the passion and energy of an accomplished team of seasoned experts, our focus is to revolutionise the standard of care in the neuromodulation space by transforming the lives of patients suffering from debilitating pain.
Reporting to the Senior Manager, Mechanical Engineering the primary role of this position is to support the mechanical engineering team on continuous improvement initiatives and executing project activities.
Accountabilities and Associated Responsibilities:
- Responsible for the DVT and process labs, which includes:
- Inducting new staff to these labs
- Maintain safe work environment
- Managing DUT and equipment owned by the mechanical engineering team and ensuring accurate records for these items are maintained
- Perform inspections, product characterisation and/or verification testing and produce documentation to appropriately capture outcomes.
- Produce complex prototypes and tools as needed for product development activities.
- Ensure that Good Documentation Practice (GDP) is followed.
- Follow established documentation structure to ensure consistency of format, style, quality, clarity, and accuracy.
- Performing all work duties in a manner that ensures the health and safety of all employees.
- Proactively identify process improvement opportunities.
Additional Expectations:
- Attend WH&S meetings as person responsible for the DVT and process labs.
Essential Requirements:
- Attention to detail and desire to develop knowledge of product development environment.
- Ability to communicate and collaborate with subject matter experts in various disciplines.
- Logical mindset, ability to work with numbers, basic understanding of product inspections and eagerness to learn more about product testing.
- Familiarity with Microsoft Office (Word, Excel).
Desirable Requirements:
- Experience in the medical device field or a similar highly regulated business environment.
- Experience managing equipment used in an engineering lab.
- Familiarity with Arena.
- Familiarity with WH&S requirements.
Salary Range:
70-85k depending on skills and experience.
At Saluda, we challenge boundaries. We innovate and think beyond the conventional. We disrupt.
Are you Ready to Join? If you would like to be part of our team developing the world's next generation of implantable device technology, contribute to making an impact on patient care, then this is the opportunity for you! Please APPLY NOW!
Applications will only be considered from candidates with the appropriate approval to work in Australia, no visa or sponsorship is available for this role.
All eligible candidates are invited to apply. We respectfully ask for no agency approaches.
Top Skills
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








