Medical Device Complaints Engineer - Quality & Compliance
DEKA Research and Development
A leading medical innovation firm in Manchester, NH, is seeking a Product Complaints Engineer to address product complaints and ensure compliance with regulatory standards. The ideal candidate will possess a biomedical engineering degree and have experience in a cGMP environment. Responsibilities include conducting evaluations, interfacing with regulatory agencies, and contributing to process improvement initiatives. Strong problem-solving and communication skills are essential for this dynamic role. Join a team dedicated to innovative medical device solutions. #J-18808-Ljbffr DEKA Research & Development
- ...companies. Responsibilities Quality assurance and compliance verification... ...S. or M.S. preferably in engineering, computer science, bioinformatics... ...quality engineering in the medical device industry or in‑vitro... ...Deep understanding of CAPA, complaint handling, Change Requests...Complaints
- ...are manufactured safely, legally, and to the required quality standards by monitoring compliance with food safety systems, customer requirements, and site... ...met Sampling, Testing & Records Carry out complaint investigation Carry out product, environmental, and raw...ComplaintsShift work
- ...Development as a Senior R&D Manufacturing Engineer, where you'll transform innovative medical devices into scalable manufacturing solutions. You... ...guide new product introductions, ensuring compliance with safety and quality standards. Your role will involve managing...Suggested
- ...in Manchester, NH, is looking for a Senior Test Engineer to influence the success of innovative medical device projects. This role involves writing test plans and... ..., evaluating devices, and contributing to quality assurance efforts in a collaborative environment....Suggested
- A leading medical device innovation firm in Manchester, NH, is seeking a Verification and Validation Test Engineer to work in a dynamic R&D environment. This role involves developing and writing test procedures, determining test coverage, and contributing to regulatory...Suggested
- ...Manchester, NH, is seeking a Director of Post Market Products to oversee post market surveillance in medical devices. The successful candidate will ensure compliance with FDA regulations and ISO standards while leading a multidisciplinary team. Requirements include a...
$20 - $23 per hour
...cleanroom production and requires hands-on experience in assembly and testing of medical devices. Candidates will work across shifts, assembling components, maintaining quality, and ensuring compliance with manufacturing standards. The ideal candidates will have strong...Temporary workShift work- ...& Development is seeking a Supplier Quality Engineer in Manchester, NH. You will lead supplier... ...and product validation, ensuring compliance with ISO 13485 standards. This role serves... ...years of relevant experience in the medical device industry. Strong analytical and...
- ...Manchester, NH is seeking a Senior Supplier Quality Engineer to oversee supplier quality... ...The role involves ensuring supplier compliance with regulatory requirements like ISO... ...Engineering with strong knowledge of medical device regulations. The position requires excellent...
$20 - $23 per hour
...Schedule: 9/80 (Every Other Friday Off) Openings: Engineering Technician: 1 opening Manufacturing Technician – Cleanroom... ...Technicians play a critical role in assembling medical devices while ensuring quality, compliance, and efficiency in a fast‑paced, regulated...Hourly payTemporary workShift workNight shiftDay shiftAfternoon shift- ...body audit. Evaluate the medical device manufacturer's Quality Management System (QMS)... ...audit readiness, risk-based compliance, and effective... ...Sterilization, Validation). CAPA, Complaint Handling, and Post-... ...Requirements Bachelor's degree in Engineering, Life Sciences, or a...ComplaintsImmediate start
- The Supplier Quality Engineer is responsible for leading supplier quality activities during... ...validation. This role ensures supplier compliance to applicable requirements, including... ...Engineering, or related role in medical device or regulated industry Strong knowledge...Contract work
- ...CurrentBody, ZIIP, and Tria — across medical devices, beauty devices, and cosmetics. Wide... ...this role suits candidates from device compliance, quality systems, international registrations,... ...Essential - Degree in a scientific, engineering, business, or regulatory discipline —...Work at officeWork from homeFlexible hours
- DEKA Research & Development in Manchester, NH, is looking for an experienced mechanical design engineer to contribute to the development of innovative medical devices. Candidates should have at least 5 years in mechanical design and be self-sufficient in managing multiple...
- ...has been continuously manufacturing high-quality materials designed to perform in the... ...excellent customer support. The Process Engineer develops and optimizes cost-effective manufacturing... ...waste, ensures safety and quality compliance, and contributes to the company’s...InternshipWork at officeFlexible hours
- ...Merrimack Manufacturing is a medical device manufacturer located in the... ...life. Position Summary The Quality Operations Specialist is responsible... ...closely with Production, Engineering, Supply Chain, and Quality... ...role in maintaining compliance with ISO 13485, applicable regulatory...Work at office
- DEKA Research & Development in Manchester, NH is seeking a Sr. Mechanical Engineer to drive innovative medical device projects. You will work collaboratively with a multi-disciplinary team, establishing design requirements and tackling challenges from concept to delivery...
- ...Technologies, is looking for a Product Complaints Engineer - Team Lead to work in a dynamic Medical Device environment. The position... ...direct impact in the Quality Management System. How you will... ...multiple projects and ensure compliance with regulations and standard...ComplaintsFor contractors
- A medical tech company located in Manchester, NH is seeking a Senior Software Quality Engineer. In this role, you will develop and support vital software tools for medical devices, collaborate with diverse teams, and ensure compliance with FDA regulations. The ideal candidate...
- ...Description InnoTECH Staffing is seeking a Senior Mechanical Engineer to develop innovative medical devices in Southern New Hampshire. This requires being... ...design, controls, and systems engineers, along with Quality, Regulatory, human factors, safety testing, and...
$75k - $90k
...specialty materials in Manchester, NH, is seeking a Process Engineer for PTFE Lamination. The role involves developing and optimizing... ...processes, improving productivity, and ensuring safety and quality compliance. Candidates should have a Bachelor's Degree in a relevant...Full time$55k - $63.25k
...coordinating room service delivery where applicable. Provide quality and compliance leadership. Responsible for supporting building inspections... ...standards. Solve issues before they become problems or complaints. Act as “Manager on Duty” when the General Manager/Executive...ComplaintsWork experience placement$130k - $140k
...management. Job Overview The Medical Information Manager serves as... ...messaging. Proofreading and Quality Control Perform meticulous proofreading... ...guidance. Regulatory Compliance Ensure all communications... ...affairs. Experience in the medical device and/or pharmaceutical...Temporary workWork at officeLocal areaImmediate startFlexible hours- ...career in the dynamic and fast-growing medical device industry. With structured training, hands... ...discussionsRespond to IT and compliance queries during the sales processAccount... ...our centralised support functions across Quality and Compliance, Logistics, Warehousing,...Contract work
- ...PMS) activities across DEKA medical device portfolio, ensuring... ...dashboards to track the status of complaint investigations, CAPA... ...analysis, and resolution in compliance with 21 CFR Part 803 and 8... ...drive accountability across engineering, quality, manufacturing, and...ComplaintsFor contractors
- ...the ibot® Personal Mobility Device, a marvel of engineering that climbs stairs,... ...maintain a high level of quality and responsiveness Ability... ...Experience with handling customer complaints Ability to maintain... ...Experience with Salesforce CRM Medical billing and coding experience...ComplaintsWork at office
- ...® Personal Mobility Device, a marvel of engineering that climbs stairs,... ...customer inquiries and complaints via phone, email,... ...clinicians and users of the medical device Assist users... ...for accuracy and compliance Monitor inventory... ...Detail, safety, and quality oriented....ComplaintsWork at office
- ...activities in a dynamic medical device research and... ...impact on the safety, compliance, and continuous improvement... ...Oversee and direct complaint handling operations,... ...consistently achieve complaint quality objectives.... ...multidisciplinary team of complaint engineers, failure analysis...ComplaintsContract workFor contractorsImmediate startWorldwide
- Granitestatemfg in Manchester, NH is seeking a Quality Engineering Manager to oversee manufacturing quality assurance, ensure product quality and compliance with strict industry regulations. This role entails driving continuous improvement and managing quality teams to...
- ...referral sources, and caregivers for a non-medical home care agency. This role is responsible... ...service updates to aides Escalate concerns, complaints, or service issues to management as appropriate Administrative & Compliance Support Maintain organized and accurate intake...ComplaintsFull timeWork at office
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