Senior Engineer, Design Quality, Software
Role details
Job location
Tech stack
Job description
The Senior Design Quality Engineer provides professional expertise for Software quality and best practices in SW development across the global organization and assists development teams in applying regulatory rigor to Agile SW development practices, including SW release and manufacturing. This individual will lead Software Quality's participation in specifying and monitoring SW manufacturing and post-market operations. The Senior Design Quality Engineer serves as a subject matter expert for the application of medical device SW regulatory standards to the Olympus SDLC, including ISO 13485, 21CFR820, IEC 62304, IEC 82304, ISO 14971, ISO 81001-2, and AAMI TIR34971/CR34971. This individual will be responsible for review and approval of documentation deliverables from assigned projects as required by the SDLC, and will support Regulatory Affairs' efforts in creating submission materials for various regulatory domains including FDA, PMDA, and EU-MDR., * Advise SW development and operations teams on Software processes and practices including SW release, manufacturing, and post-market operations.
- Working with global cross functional teams, explore and implement harmonization of SW manufacturing and operations processes across different Olympus legal entities
- Advise Olympus as a Subject Matter expert on regulations around SW manufacturing and cloud operations.
- Advise Olympus as a Subject Matter expert on regulations around SW post market monitoring for Medical and Health Software products.
- Collaborate on the update of SDLC and operations processes and activities for the manufacture, distribution, and operations monitoring of SW.
- Collaborate on the update of SDLC and operations processes and activities for the inclusion of product security in SW operations environments.
- Represent Olympus's SW manufacturing and post-market operations QMS during inspections and audits.
- Perform capability audits of software projects.
- Establish and monitor performance metrics for SW manufacturing and post-market activities.
- Support the establishment of a dashboard for post market operations for SW products.
- Communicates significant issues to senior management, including appropriate containment and correction activities, as applicable.
Requirements
- Undergraduate (BS) Degree in engineering, computer science, life sciences, or other related degree field.
- Minimum of 8 years of experience in the field of software development, software testing, or systems engineering, or 6 years for advanced degree.
- Minimum of 5 years of experience in a medical device setting.
- Experience in the application of relevant standards to medical device software manufacturing, release, and post-market operations.
- Experience in working across national and cultural boundaries.
- Demonstrated capability to lead and train a large and diverse, multinational community with multiple stakeholders, working in a collaborative, coaching, mentoring and/or influencing capacity.
- Strong teamwork and communication skills to work effectively on cross-functional project teams, Interacting with a diversity of disciplines such as R&D, Quality Engineering, Regulatory Affairs, etc.
- Independent organizational and time management skills is required.
- Strong verbal and written communication skills in English.
- Will work with global teams; availability will include working across the associated time zones; some flexibility in work hours will be expected. Travel up to 15% of the time. Candidate will be able to work from home on a regular basis.
Preferred:
- An Advanced degree such as an MS or PhD is preferred.
- Experience in interacting with Regulatory Authorities is preferred.
- Japanese communication skill are an optional, added plus factor.
Benefits & conditions
- Competitive salaries, annual bonus and 401(k)* with company match
- Comprehensive medical, dental, vision coverage effective on start date
- 24/7 Employee Assistance Program
- Free live and on-demand Wellbeing Programs
- Generous Paid Vacation and Sick Time
- Paid Parental Leave and Adoption Assistance*
- 12 Paid Holidays
- On-Site Child Daycare, Café, Fitness Center**
Connected Culture you can embrace:
- Work-life integrated culture that supports an employee centric mindset
- Offers onsite, hybrid and field work environments
- Paid volunteering and charitable donation/match programs
- Employee Resource Groups
- Dedicated Training Resources and Learning & Development Programs
- Paid Educational Assistance
*US Only
**Center Valley, PA and Westborough, MA
Are you ready to be a part of our team?
Learn more about our benefits and incentives: https://www.olympusamerica.com/careers/benefits-perks.
The anticipated base pay range for this full-time position in this location is $95,904.00 - $129,470.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements).