Senior Electrical Engineer IV — Medical Device; Onsite — Arden Hills, MN – E

Saint Paul, United States | Posted on 02/04/2026

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at  and follow us on Linked In:

Our F500 Medical Device client has an exciting opportunity for a Senior Electrical Engineer IV.

Receives minimal technical direction/review on a broad scope of complex client projects for design analysis of active implantable devices. Working independently, or as member of a team; develops protocols, executes testing of specifications and designs, completes statistical analysis, and documentation within the quality system.

Designs, develops, debugs, modifies, and tests electrical circuits and systems by using current tools, analysis techniques, and technologies.

Documents electrical development by writing documents, reports, memos, change requests. Methods used are determined by approved procedures and standards.

Tracks electrical development effort by creating and maintaining records in the approved tracking management tool to include, utilizing multiple version control, defect tracking, and peer review tools including Accurev, JIRA and Windchill.

Solves engineering problems by analyzing the situation and recommending corrective or alternative actions.

Analyzes, evaluates, verifies, requirements, circuits, and systems by using engineering practices.

Investigates, research, selects electronic circuits, components, tools, equipment and practices.

Ability to perform design analysis and exploratory testing.

Ability to work with electrical and mechanical hardware and associated tools and infrastructure.

Able to write final evaluation reports and work with regulatory group to satisfy the requirements for external regulatory agencies.

Establishes and promotes a work environment that supports the Quality Policy and Quality System. Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Solves a range of problems of varying scope and complexity, generally applying existing solutions, while exercising autonomy to propose alternatives understanding their impact on the business or apply judgment based on experience to develop new solutions.

Works independently guided by company policies, guidelines and procedures, receiving guidance on complex and unprecedented problems.

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

• Bachelors required in Electrical Engineering (plus 5+ year experience) or Masters (plus 3+ year experience)
• Ability to collect, organize, synthesize, and analyze data; summarize findings; develop conclusions and recommendations from all stakeholders using all sources of data.
• Ability to analyze test results and perform risk analysis.
• Ability to interpret and research requirements, specifications, and input/output processes.
• Experience with change management and issue tracking tools such as JIRA, Accu Rev, Windchill etc.
• Requires in-depth conceptual, practical and technical and/or functional knowledge of principles and theories of board level electrical engineering and general understanding of related job functions

• 3+ years of experience in hardware engineering.
• 3+ year experience automated and manual testing in regulated industry, preferably in active implantable medical device domain.
• 2+ year experience in system development lifecycle process including formalized processes and procedures.
• Create test protocols and automate tests using Python and other relevant tools.
• Create protocols, automate tests, general experience in Perl, Python, HTML, scripting or equivalent

Schedule:

08:00:

AM - 04:30:

PM

Contract Length: 12 months with Possible Extension (2/23/2026 - 2/23/2027)

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.