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
- A leading medical device firm in Manchester, NH seeks a Quality Engineer for their Quality Department. In this dynamic role, you will provide quality guidance and support compliance with regulations like 21 CFR 820 and ISO 13485. The ideal candidate will have a Bachelor...Suggested
- Merrimack Manufacturing is a medical device manufacturer located... ...Position Summary The Quality System Specialist‑... ...System (QMS) in compliance with ISO 13485 and applicable... ...activities including complaint management, internal... ...in Quality, Engineering, Life Sciences, Manufacturing...ComplaintsWork at office
- Complaint Handling Specialist DEKA Research & Development,... ...to support our product quality and regulatory compliance efforts. In this role, you... ...FDA Quality Systems and Medical Device Reporting regulations (2... ...day through thoughtful engineering, design, and manufacturing...ComplaintsWork at office
- ...Sr. QA Specialist - Supplier Quality Location: Bedford, New... ...QA Dir, Quality Systems & Compliance Responsible For (Staff):... ...supplier non-conformance and complaint handling Responsible for... ...in a pharmaceutical/biotech/medical device environment is a must Thorough...ComplaintsContract work
- DEKA Research and Development in Manchester, NH, is seeking a Complaint Handling Specialist to support product quality and compliance efforts. You will manage complaint documentation, ensure compliance with FDA and QMS requirements, and maintain organized documentation...Complaints
- DEKA Research & Development is looking for a detail-oriented Complaint Handling Specialist to support product quality and regulatory compliance in Manchester, NH. You will manage complaint documentation and data entry, ensuring compliance with FDA and QMS requirements....Complaints
- A medical device manufacturer located in Manchester, NH, is seeking a Senior Manufacturing Engineer to drive improvements in production processes. The successful candidate will lead technical projects, manage a team, and apply Lean Manufacturing principles. Ideal candidates...
- DEKA Research & Development in Manchester, NH is seeking a Senior Test Engineer. This role involves creating test plans and procedures for electro-mechanical devices, primarily in the medical field. The ideal candidate has a BS in relevant engineering fields and over 3...
- 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...
$22 per hour
...Area Director is the execution engine of Healthy Kids Programs'... ...are choosing to re-enroll Compliance - All sites operate in full... ...2. Enrollment & Program Quality Monitor enrollment at... ...building-level concerns and complaints quickly; resolve issues at the...ComplaintsHourly payPart timeSummer workWork at officeImmediate start- ...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...
- ...Manufacturing in Manchester seeks a Quality System Specialist to support... ...13485. The role will manage complaint handling, conduct internal... ..., and monitor regulatory compliance to improve quality processes... ...or assurance within the medical device industry. Strong analytical...Complaints
- ...the development and implementation of the training system in compliance with ISO 13485. This role requires managing training processes... ...regulatory standards. Ideal candidates will have a degree in Quality, Education, or related fields, along with 2-5 years of experience...
- ...The Supplier Quality Engineer (SQE) supports supplier quality activities across both New Product Introduction... ...sustaining manufacturing operations within a regulated medical device environment. This role ensures supplier compliance to applicable requirements, including 21 CFR...Remote work
- ...Merrimack Manufacturing is a medical device manufacturer located in the... ...system within a medical device Quality Management System (QMS)... ...documented, and maintained in compliance with regulatory and internal... ...Human Resources, Manufacturing, Engineering and Regulatory Affairs to...Work at office
$90k
...Job Title: NPI Quality Engineer Location: Manchester, NH Type: Temp-to-Perm Salary... ...within a fast-paced, innovative medical device manufacturing environment. This role... ...in launching new products, ensuring compliance with regulatory standards, and driving...Permanent employmentTemporary workImmediate startMonday to Friday- ...Technologies,is looking for a Product Complaints Engineer to work in a dynamic Medical Device Research and Development... ...significant direct impact in the Quality Management System. How you will... ...multiple projects and ensure compliance with regulations and standard operating...ComplaintsContract workFor contractors
$115k - $135k
Fresenius Kabi USA, LLC is looking for a Sr Engineer, Mechanical in Manchester, NH. In this hybrid role, you'll work on developing mechanical systems for their products while collaborating closely with other team members. Candidates should have over 5 years of experience...- A leading medical device company in Manchester, NH is seeking a Senior Manufacturing Engineer to transform innovative designs into scalable manufacturing solutions. You will evaluate design manufacturability, lead DFM reviews, and manage product development from prototypes...
- A medical device manufacturer in Manchester, NH, is looking for a Manufacturing Engineer to enhance production processes. The ideal candidate will work collaboratively with... ...supports the improvement of manufacturing quality and efficiency. #J-18808-Ljbffr Merrimack Manufacturing
- 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...
$75k - $90k
...has been continuously manufacturing high‑quality materials designed to perform in the... ...support. Job Type: Full‑time Process Engineer - PTFE Lamination The Process Engineer develops... ...waste, ensures safety and quality compliance, and contributes to the company’s ongoing...Full timeInternshipWork at officeFlexible hours- A leading medical device manufacturer in Manchester is looking for a Controls Engineer to design and optimize control systems within the production environment. The role requires 3-5 years of experience in PLC programming and troubleshooting. Candidates should possess...
- ...the ibot® Personal Mobility Device, a marvel of engineering that climbs stairs,... ...engineering discipline preferred. Medical device experience... ...Attention to detail, safety and quality oriented, with ability to... ...Experience with handling customer complaints Outstanding customer...ComplaintsWork at office
- 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...
$20 - $23 per hour
...Schedule: 9/80 (Every Other Friday Off); Openings: Engineering Technician: 1 opening Manufacturing Technician -... ...Manufacturing Technicians play a critical role in assembling medical devices while ensuring quality, compliance, and efficiency in a fast‑paced, regulated...Temporary workShift workNight shiftDay shiftAfternoon shift- ...Location: Manchester - MHT Department: Quality Assurance Reporting To: QA Manager/... ...QA Training personnel to support compliance with GMP and regulatory requirements. The... ...industry (pharmaceutical, biotech, or medical device). ~ Experience with electronic Learning...
- ...practice to independently initiate patient workups including labs, EKG, imaging, and medications based on chief complaint Operate unit equipment including Alaris pumps, Pyxis, Lucas Device, Hotline Rapid Infuser, and ultrasound for IV access Document accurately using...ComplaintsWeekly payFull timeContract workImmediate startWeekend work
- Overview Principal Engineer - Medical Devices (Hybrid) job at Gallin Associates. Manchester, NH. CLIENT CANNOT TRANSFER OR SPONSOR WORK VISA AUTHORIZATION... ...development team of Electrical, Software, Mechanical, and Quality engineering. Qualifications Bachelor of Science in...Visa sponsorshipWork visa3 days per week
- ...Description Job Description The Supplier Quality Engineer is responsible for leading supplier... .... This role ensures supplier compliance to applicable requirements, including... ...Quality Engineering, or related role in medical device or regulated industry ~ Strong...Contract work
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