Software Quality Assurance Engineer
SolventumAbout the role
Job Description:
3M Health Care is now Solventum
At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.
We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.
The Impact You’ll Make in this Role
As a(n) Software Quality Assurance Engineer you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:
- Leads software quality assurance activities throughout medical device software life cycle, including creating software quality assurance plans, performing software configuration management and change control activities, writing reports, performing gap assessments against applicable regulations and industry standards.
- Implements standard operating procedures for medical device software engineering, takes an active role in continuous improvement of the medical device software engineering process, including authoring, reviewing, and approving procedures, work instructions and templates.
Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:
- High School Diploma with 8 years of experience in medical device software quality or other regulated industry with equivalent software safety and security standards OR Bachelor’s degree in Computer Science or equivalent with a minimum of 3 yrs of experience in medical device software quality or other regulated industry with equivalent software safety and security standards OR Master’s degree in Computer Science or equivalent with more than one year of experience in medical device software quality or other regulated industry with equivalent software safety and security standards
Additional qualifications that could help you succeed even further in this role include:
- Working knowledge of medical device software regulations (FDA, EU and other agencies) as well as medical device related standards such as ISO 13485, ISO 14971, IEC 62304 amongst others.
- Working knowledge of C language preferred
- Excellent verbal and written communication skills, strong problem-solving ability and attention to detail
- Ability to effectively manage multiple simultaneous tasks and priorities and perform under a dynamic environment with parallel product releases and multiple project teams
- Ability to deal effectively with all employees and external business contacts while conveying a positive, service-oriented attitude.
Work location:
- Remote
Travel: May include up to [5%][domestic/international]
Relocation Assistance: May be authorized
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
Supporting Your Well-being
Solventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.
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