Quality Systems Engineer – Software Compliance

Posted Yesterday
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Manchester, NH
Junior
Healthtech • Biotech
The Role
As a Quality Systems Engineer at DEKA, you will focus on improving quality and compliance in software development by refining SOPs, leading internal investigations, ensuring compliance with FDA and ISO standards, and collaborating with cross-functional teams. Your role also involves technical writing and project management.
Summary Generated by Built In

Join our dynamic team at DEKA and be at the forefront of driving quality excellence! As our Quality Systems Engineer, you'll be a key player in our collaborative environment, working hand-in-hand with cross-functional teams to ensure the highest standards of quality and compliance.
As a Quality Systems Engineer, you will contribute in the following areas:

  • Attain a comprehensive understanding of FDAs medical device software development requirements, leveraging this knowledge to champion improvement initiatives within the Quality Management System (QMS) and actively seeking opportunities to enhance DEKAs software development procedures.
  • Develop and revise Standard Operating Procedures (SOPs) and associated change controls, ensuring alignment with regulatory requirements to support DEKAs software development processes.
  • Lead collaborative efforts to drive internal investigations and improvements by ensuring comprehensive analysis and appropriate solutions are implemented by cross-functional teams.
  • Ensure compliance with FDA Part 820 and ISO 13485 regulatory standards, maintaining the integrity and effectiveness of the DEKA QMS.
  • Review and approve quality records to ensure accuracy, completeness, and compliance with regulatory requirements.

As a key contributor to our team, you will demonstrate the following skills:

  • Technical Writing: Proficient in conveying complex technical information clearly and concisely to as variety of audiences.
  • Aptitude for Learning Technical Information: Ability to comprehend and apply technical concepts effectively.
  • Effective Communication: Ability to articulate problems and solutions with clarity and precision to a diverse, cross-functional team with varying levels of technical aptitude.
  • Project Coordination/Management: Skilled in planning, executing, and managing projects with varying timelines.
  • Problem Solving: Embrace challenges and find creative solutions.
  • Collaboration: Effectively collaborate with various teams and departments, sharing ideas, taking initiative and proactively contribute to achieve common objectives. Work to maintain a positive attitude, fostering a supportive and productive work environment.
  • Attention to Detail: Display exceptional accuracy and precision in all tasks.
  • Reliability: Consistently delivering high-quality work and demonstrating dedication to your role.
  • Excellent at utilizing or the ability to quickly learn applications, including Excel, Word, and Visio.

Required Training / Knowledge: 

  • BS/MS in Science or Engineering
  • Preferred 2+ years’ experience in quality systems management, medical device, or a similar regulated environment
  • Experience with software development (medical device preferred)
  • Strong written/verbal communication skills
  • Excel, Word, Visio skills
  • Technical writing experience
  • Project coordination/management skills
  • Aptitude for learning technical information
  • Must be able to work onsite Monday-Friday
  • Nice to have:
    • Knowledge of FDA’s Quality System Regulation
    • Knowledge of ISO 13485 and related standards

About DEKA:

One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.

Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.


 #LI-Onsite
 

The Company
HQ: Manchester, NH
670 Employees
On-site Workplace
Year Founded: 1982

What We Do

DEKA is one of the leading research and development companies in the country and is the birthplace of some of the most innovative and life-changing products of our time. For over thirty years, DEKA Research & Development Corp. has made Manchester, New Hampshire home. Located about an hour from Boston, the beach, and the mountains, we are situated in the beautiful and historic Amoskeag Millyard buildings located in downtown Manchester.

DEKA continues to be a place where no idea seems too big and where creativity and crazy cool gizmos reign supreme. The engineers, technicians, machinists, designers and all of the other folks who make up DEKA are some of the most creative and innovative professionals you could ever hope to meet. It's a place where one crazy idea can end up being the next greatest invention. At DEKA we embrace the spirit of innovation and constantly aim to turn the impossible into a reality.

DEKA is filled with people who are driven to be among the best and brightest in their field of work. It’s a concentrated bunch of really smart thinkers, doers and problems solvers, who are driven to using innovative design solutions and state-of-the-art technology to improve lives. We all see endless possibilities in the power of technology to do good. Employees have the opportunity to work on diverse projects that have a positive, enduring impact on millions of people worldwide. We are growing! We're always seeking passionate individuals to join our growing team of evolved thinkers.

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