DEKA

35 Deka Jobs Hiring Near You

CAD Designer

Manchester, NH ยท On-site

$27 - $37/hr

As a CAD Designer at DEKA Research & Development Corp., you will partner with both Mechanical and Electrical Engineering teams to support the full spectrum of CAD Department activities. In this role ...

DEKA Research & Development, located in Manchester, NH, is seeking a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on ...

Senior Electrical Engineer

Manchester, NH ยท On-site

$107K - $139K/yr

Understand and follow DEKA processes, design control practices, and documentation requirements * Manage external design partners and suppliers * Manage your time effectively across multiple ...

Device Coordinator

Manchester, NH ยท On-site

$19.25 - $26/hr

DEKA Research & Development is searching for a Device Coordinator to join our growing team. This role will be directly supporting the Lead Test Technician in maintaining the use of test equipment ...

DEKA Research & Development is seeking a skilled PCB Layout Designer to join our engineering team. The successful candidate will be responsible for translating electrical schematics into optimized ...

DEKA Research and Development is looking for a DevSecOps Engineer who wants their work to matter: someone who takes pride in building secure, reliable pipelines that let engineers ship faster and ...

DEKA is seeking a reliable and detail-oriented Test Technician to support Cleaning Durability Testing initiatives. This hands-on role involves executing and documenting repetitive cleaning cycles ...

DEKA Research and Development, housed in Manchester, NH, is looking for a dynamic, results driven and inventive Senior Software Quality Assurance Engineer to support the development of life-changing ...

Quality Engineer

Manchester, NH ยท On-site

$71K - $92K/yr

DEKA R&D has an immediate opening for a Quality Engineer to work in the Quality Department in a dynamic Medical Device Research and Development environment. The position reports to the Quality ...

Warehouse Associate

Manchester, NH ยท On-site

$16 - $19/hr

DEKA Research and Development, on behalf of Millyard Advanced Medical Products, a Manufacturer of Record for innovative medical devices, has an immediate opening for an Experienced Warehouse ...

DEKA R&D, on behalf of Millyard Advanced Technologies is looking for a Junior Product Complaints Engineer to work in a dynamic Medical Device Research and Development environment. The position ...

Warehouse Associate

Manchester, NH ยท On-site

$15.50 - $18.50/hr

DEKA Research and Development, on behalf of Millyard Advanced Medical Products, a Manufacturer of Record for innovative medical devices, has an immediate opening for an Experienced Warehouse ...

DEKA Research and Development, housed in Manchester, NH, is looking for an experienced mechanical design engineer to participate in the development of innovative medical devices. They will work as ...

Electromechanical Technician

Manchester, NH ยท On-site

$24.75 - $31.25/hr

DEKA is looking for a hands-on, detail-oriented Engineering Service Technician to help keep our medical devices and test equipment running smoothly. In this role, you'll work with different groups ...

Senior Manufacturing Engineer

Manchester, NH ยท On-site

$90K - $124K/yr

As a Senior Manufacturing Engineer at DEKA, you'll play a critical role in transforming innovative medical device designs into scalable, high-quality, and regulatory-compliant manufacturing solutions.

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DEKA Jobs Information

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Infographic showing various job openings at Deka in the United States as of July 2026, with employment types broken down into 97% Full Time, and 3% Temporary. Highlights an 100% Physical job distribution.

Quality Systems Engineer - CAPA and Process Improvement

DEKA

Manchester, NH โ€ข On-site

Full-time

Posted 9 days ago


Job description

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:
  • Own and manage the end-to-end CAPA process, from intake and triage through investigation, root cause analysis, corrective/preventive action planning, and effectiveness verification.
  • Facilitate cross-functional CAPA review meetings, ensuring teams identify systemic issues and align on appropriate remediation strategies.
  • Ensure each CAPA is supported with objective evidence, clear problem statements, and traceability to impacted processes, products, or quality records.
  • Maintain CAPA documentation in alignment with regulatory expectations, ensuring timely closure, audit readiness, and linkage to risk management where applicable.
  • Monitor CAPA trends and performance metrics to identify recurring issues and drive continuous improvement.
  • Support training and mentorship of team members on CAPA expectations, best practices, and root cause analysis tools.
  • Own the development and revision of Standard Operating Procedures (SOPs) and associated change controls to ensure they align with regulatory requirements and support QMS compliance.
  • Ensure ongoing compliance with FDA 21 CFR Part 820 and ISO 13485, maintaining the integrity and effectiveness of the DEKA QMS.
  • Develop a strong working knowledge of DEKA's QMS processes and use this expertise to identify and implement system improvements.
  • Review and approve quality records, ensuring accuracy, completeness, and adherence to applicable requirements.
  • Conduct internal audits and support auditor training efforts to promote audit readiness and compliance with regulatory requirements.
  • Support external audits (e.g., FDA, ISO, customer audits) by preparing documentation, facilitating audit logistics, and responding to auditor requests in real time.
As a key contributor to our team, you will demonstrate the following skills:
  • Strong technical writing skills: you can translate complex concepts clearly for diverse audiences.
  • A natural curiosity and ability to quickly grasp technical systems, workflows, and requirements.
  • Clear, confident communication: you know how to explain problems and solutions across a range of technical backgrounds.
  • Solid project coordination and follow-through: you're organized, dependable, and keep work moving forward.
  • A proactive problem-solver mindset: you ask the right questions, challenge assumptions, and help teams find solutions.
  • Collaborative energy: you contribute, share ideas, and maintain a constructive, can-do attitude.
  • Precision and attention to detail: your work is thorough and consistent.
  • Reliability: you take ownership, meet deadlines, and follow through.
Required Training / Knowledge:
  • BS/MS in Engineering, Life Sciences, or a related field
  • 3+ years of experience in a quality systems role in a regulated industry, ideally medical devices
  • Working knowledge of FDA QSR (21 CFR Part 820) and ISO 13485
  • Proficiency with Microsoft Excel, Word, and Visio (or ability to learn quickly)
  • Strong verbal and written communication skills
  • Experience in project coordination and technical writing

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 and 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.