Senior Electrical Engineer IV — Medical Device (Onsite — Arden Hills, MN) Contract – Possible Extension

Pharmavise Corporation; Saint Paul (MN); On-site; USD 110,000 - 150,000; Full time

Job summary

Pharmavise Corporation in Saint Paul, MN, seeks a Senior Electrical Engineer IV to perform design analysis of active implantable devices, working independently or in a team to develop protocols, execute tests, analyze data, and document findings within the quality system.

You will evaluate circuits and systems, perform exploratory testing, and create final evaluation reports while coordinating with regulatory teams to meet external requirements.

Qualifications

• Bachelor's degree in Electrical Engineering (5+ years experience) or Master's (3+ years experience)
• Experience with change management and issue tracking tools such as JIRA, AccuRev, Windchill
• Ability to perform design analysis and exploratory testing
• Strong documentation and reporting to regulatory groups
• Knowledge of quality systems and patient safety principles

Responsibilities

• Designs, develops, debugs, modifies, and tests electrical circuits and systems for active implantable devices
• Documents electrical development through reports and change requests
• Maintains records using tracking tools and version control
• Analyzes requirements, circuits, and systems using engineering practices
• Collaborates with regulatory to satisfy external regulatory agencies
• Builds a quality-focused work environment and adheres to policies

Skills

Electrical engineering design

Problem solving

Documentation

Statistical analysis

Independent work

Team collaboration

Education

Bachelor's degree in Electrical Engineering

Master's degree in Electrical Engineering

Tools

JIRA

AccuRev

Windchill

Python

Perl

HTML scripting

Job description

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 www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp

Job Description

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

Job Summary:

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.

Responsibilities and Job Requirements:

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

Quality Systems Duties and Responsibilities:

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, AccuRev, 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

Preferred requirements:

• 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

Other Details:

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.