Medical Device Software Verification Engineer

Bausch & Lomb GmbH; Missouri; On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) plan and company match

Tuition reimbursement programs

Well-being benefits

Paid vacation

Job summary

Bausch & Lomb GmbH is seeking a Systems Engineer to support medical device programs with an emphasis on software verification and validation. This role includes responsibilities like regression testing, transitioning software documentation, and contributing to cybersecurity activities. Ideal candidates will have a Bachelor's degree in a relevant field and 3–7 years of engineering experience.

Being part of a dedicated team, you will assist with compliance to regulatory requirements while managing multiple projects involving both internal documentation development and external supplier support.

Qualifications

• Bachelor's degree in Engineering (Computer, Software, Systems, Biomedical, or Electrical) or equivalent.
• 3–7 years of engineering experience with a focus on software.
• Strong communication and organizational skills required.

Responsibilities

• Plan and execute full regression testing for software releases.
• Perform software verification and validation per Quality Management System.
• Transition third-party software documentation in-house.

Skills

Software Verification and Validation

Cybersecurity

Engineering Management

Scripting and Test Automation

Documentation Development

Education

Bachelor's degree in Engineering or Computer Science

Tools

MS Office

Aras PLM

D2

Job description

Bausch & Lomb GmbH is seeking a Systems Engineer to support medical device programs with an emphasis on software verification and validation. This role includes responsibilities like regression testing, transitioning software documentation, and contributing to cybersecurity activities. Ideal candidates will have a Bachelor's degree in a relevant field and 3–7 years of engineering experience.

Being part of a dedicated team, you will assist with compliance to regulatory requirements while managing multiple projects involving both internal documentation development and external supplier support.