Senior Mechanical Engineer (Biocompatibility, Packaging, and Sterilization)

Saluda Medical•Minnetonka, MN

12h•Onsite

About The Position

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 Sr. Mechanical Engineer is a key technical leader within the US-based New Product Development team. Reporting to the Head of ME, this role provides end-to-end ownership of biological safety, materials evaluation, sterilization strategy, and packaging development across the full product lifecycle. This position partners closely with R&D, Quality, Regulatory, Manufacturing, and external test laboratories to ensure Saluda’s implantable devices meet global regulatory expectations, including FDA and EU MDR. The role also supports investigations, materials assessments, and the development of new mechanical designs and manufacturing methods.

Requirements

Bachelor’s degree or higher in Materials Science, Mechanical Engineering, Biomedical Engineering, or related field.
Strong understanding of biocompatibility, sterilization, materials science, and packaging principles.
Excellent written and verbal communication skills, with the ability to convey complex technical information clearly.
Demonstrated problem-solving ability and experience conducting detailed engineering investigations.
Experience working within a QA-controlled, regulated medical device environment.
Collaborative, team-oriented mindset with the ability to work across global functions.

Nice To Haves

Working knowledge of FDA, EU MDR, ISO 10993, ISO 11135/11137, ISO 11135/11137, ISO 11607, and related standards.
Experience in neuromodulation, implantable devices, or active medical systems.
Prior experience with chemical characterization, toxicology, or sterilization validation.

Responsibilities

Lead biological safety strategy for all patient-contacting components in accordance with ISO 10993, ISO 14971, FDA guidance, and EU MDR.
Author and approve Biological Evaluation Plans (BEPs), Biological Evaluation Reports (BERs), toxicological assessments, and supporting documentation.
Oversee chemical characterization, extractables/leachable assessments, and toxicological risk evaluations.
Provide SME guidance during design controls, material selection, process development, and change control.
Coordinate and technically manage external laboratories performing biocompatibility and microbiological testing.
Develop and maintain sterilization strategies for implantable devices, including EO, gamma, or other validated modalities.
Evaluate sterilization residues, cleaning processes, and microbiological considerations to ensure patient safety.
Support sterilization validation activities, documentation, and regulatory submissions.
Partner with manufacturing to ensure sterilization processes remain compliant, robust, and audit-ready.
Lead packaging material selection, sterile barrier system development, and packaging design improvements.
Support packaging validation, including seal integrity, transit testing, and aging studies.
Ensure packaging solutions meet ISO 11607 and global regulatory requirements.
Collaborate with suppliers and internal teams to resolve packaging-related issues and drive continuous improvement.
Conduct materials assessments, including evaluation of polymers, metals, adhesives, coatings, and surface treatments.
Lead feasibility studies for new materials, processes, and manufacturing technologies supporting next-generation products.
Support mechanical design development and contribute to engineering specifications, drawings, and verification activities.
Provide technical leadership for issue investigations, including root-cause analysis, documentation, and corrective actions.
Work closely with R&D, Quality, Regulatory, Clinical, and Manufacturing teams to ensure alignment across programs.
Provide expert input for global regulatory submissions, audits, inspections, and CAPA activities.
Ensure all documentation is complete, traceable, and compliant with Saluda’s quality system.