Senior Software Quality Engineer — Medical Device; Onsite — Maple Grove, MN

Senior Software Quality Engineer — Medical Device (Onsite — Maple Grove, MN) Possible Contract Extension

Maple Grove, United States | Posted on 08/14/2025

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:

Job Summary:

Develops, establishes and maintains software quality engineering methodologies, programs, systems, and practices which meet Client, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate software quality goals and priorities. Provides focused software quality engineering support within new product development, operational, or system/services support. Functional Engineering Roles include:
Software Engineering, IT.

• Provides leadership role on championing departmental or cross-functional software development/programming/testing/validation/verification quality initiatives.
• Provides project direction, coaching, and mentoring for engineering and technical team personnel.
• Proactively investigates, identifies, and implements best-in-class Software Quality practices.
• Mentor for technical guidance for identifying and resolving software quality issues.
• Identifies and implements effective software quality systems to support the development, qualification, and on‑going manufacturing of products to meet or exceed internal and external requirements.
• Leads in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external software quality requirements.
• Acts as an effective leader or team member in supporting software quality disciplines, decisions, and practices.
• Applies sound, systematic problem‑solving methodologies in identifying, prioritizing, communicating, and resolving software quality issues.
• Assures the development and execution of streamlined business systems which effectively identify and resolve software quality issues.
• May manage small to medium‑sized projects by applying basic project management methodology (e.g., project plan, schedule, budget, etc.).

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

• 9‑11 Years of Experience with a BS Engineering degree (Software Engineering degree preferred)
• 7‑8 Years of Experience with a MS degree
• Has experience leading large teams in Software testing
• Has an understanding of Software test review process
• Has experience in Software test architecture
• Has experience automation and manual test procedures for medical device environment
• Understands IEC‑62304 standards in relation to Software verification and validation

• Schedule:
  
  08:00 AM - 04:30 PM CDT
• Work Setup:
  Onsite in Maple Grove, MN
• No Travel Requirements
• Contract Length: 12 Months (September 8, 2025 – September 7, 2026) with Possible Contract Extension

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.