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DEKA Research & Development Corp.

Independent R&D lab developing medical devices

Product Complaints Engineer

Full-TimePosted on 8/27/2026
No salary listed
Mid
Bachelor's
Manchester, NH, USA
In Person
Biology & BiotechRegulatory & Quality (Life Sciences)

About the job

Requirements
  • A bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Quality Engineering, or a related technical discipline is required.
  • A minimum of 3–5 years of experience in a regulated medical device, pharmaceutical, or life sciences environment is required, with direct responsibility for complaint investigations, product quality investigations, product analysis, and complaint closure activities.
  • Demonstrated experience conducting complaint investigations, determining root cause, documenting investigation results, and independently driving records to closure in compliance with established timelines.
  • Working knowledge of FDA Quality System Regulations, Medical Device Reporting requirements, and applicable standards, including 21 CFR Parts 803 and 820.
  • Strong technical troubleshooting, analytical, and problem-solving skills, including the ability to assess complex product performance issues and identify potential failure modes.
  • Strong time management skills, including the ability to manage a high-volume complaint workload while meeting regulatory and internal closure targets.
  • Technical writing skills with the ability to prepare clear, concise, and compliant investigation reports.
  • Strong written and verbal communication skills, including the ability to interact effectively with Quality, Regulatory, Engineering, Manufacturing, Clinical, and Customer Support teams.
  • Ability to work independently, make sound decisions based on available evidence, and maintain compliance with regulations, procedures, and quality system requirements.
Responsibilities
  • Review complaints related to potential medical device issues.
  • Perform product complaint evaluations with minimal direction using experience and product knowledge.
  • Ensure complaint documentation follows Good Documentation Practices, meets Quality Management System requirements, and complies with U.S. Food and Drug Administration regulations and other regulatory requirements.
  • Identify and make decisions regarding medical device reporting to regulatory agencies.
  • Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies.
  • Participate in audits and CAPA investigations related to complaint handling.
  • Work with the forensic investigation team to align product investigations related to complaints.
  • Generate reports to identify areas of process improvement.
  • Develop product training aids.
  • Contribute independently while collaborating with team members and departments needing product complaint information.
  • Serve as a subject matter expert on complaint handling.
  • Perform other related duties as assigned under management supervision.
Desired Qualifications
  • Experience with ISO 13485.
  • Experience evaluating product complaints for reportability and supporting regulatory submissions.
  • Experience using electronic quality management systems, complaint handling systems, and platforms such as Salesforce.
  • Ability to thrive in a fast-paced, changing environment.

About the company

D

DEKA Research & Development Corp.

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DEKA Research & Development Corp. is a leading engineering R&D lab in Manchester, New Hampshire that develops a wide range of practical technologies and devices. It operates by interdisciplinary teams of engineers, machinists, designers, and technicians who take ambitious ideas and turn them into tangible products using advanced design and manufacturing methods. The company differentiates itself through its culture of hands-on experimentation, diverse project portfolio, and a track record of bringing to market or translating ideas into real-world applications. Its goal is to create technologies with a positive, lasting impact on people’s lives by solving meaningful problems.

Company Size

501-1,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Manchester, New Hampshire

Founded

1982

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Simplify's Take

What believers are saying

  • Diatech acquisition on October 7, 2025 deepened DEKA’s diabetes delivery stack.
  • Emergex collaboration keeps DEKA’s intradermal applicator active across 2026 biotech pipelines.
  • Revelio counted 872 employees in March 2026, and hiring stayed active.

What critics are saying

  • Sequel Med Tech drives twiist commercialization; any 2026 launch miss starves DEKA royalties.
  • Dean Kamen’s February 2026 Epstein scrutiny pressures recruiting, partnerships, and nonprofit ties.
  • DEKA’s revenue depends on a narrow medical-device portfolio; one regulatory failure hurts everything.

What makes DEKA Research & Development Corp. unique

  • Dean Kamen’s 1982 engineering bench produced LUKE, iBOT, and twiist.
  • DEKA owns core infusion and microneedle IP, not just outsourced design.
  • FDA cleared twiist in 2025, proving repeatable regulated-device execution.

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Benefits

  • Hybrid Work Options

Company News

Emergex Vaccines Holding Limited
Jan 16th, 2024
Emergex Announces R&D Collaboration with DEKA Research & Development Corp. for Assessment of Emergex's Immunotherapeutic Candidates with DEKA's Intradermal Therapeutic Applicator

- Emergex has entered into an agreement with DEKA Research & Development ('DEKA') to assess the compatibility of Emergex's T cell-priming set-point immunotherapeutic candidates with DEKA's Intradermal Therapeutic Applicator.

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Oct 13th, 2022
Revolutionary And Affordable New Robotics System Makes Debut At 2022 First Global Challenge = A Win For Stem Equity

The XRP robot kits can help democratize robotics by getting younger generations excited about STEM and making the field of robotics more affordable and accessible in all parts of the world. The XRP robot kits can help democratize robotics by getting younger generations excited about STEM and making the field of robotics more affordable and accessible in all parts of the world

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