QA Engineer II - Medical Devices & Compliance
Teleflex
Teleflex is seeking a Quality Assurance Engineer to support quality systems in Mansfield, Massachusetts. You will drive continuous improvement initiatives, ensure compliance with FDA and ISO 13485 standards, and oversee quality in manufacturing processes. The ideal candidate will have a Bachelor’s Degree in Engineering or a related field, alongside at least 3 years of Quality Assurance experience in medical device manufacturing. Familiarity with SOP creation and compliance is crucial. Competitive benefits package included. #J-18808-Ljbffr Teleflex
- Smith & Nephew is seeking a Manufacturing Engineer II in Mansfield, MA, to focus on injection molding for medical device production. This pivotal role involves hands-on process optimization, mold maintenance, and collaboration on design for manufacturability. The ideal...Suggested
- Teleflex is seeking a Design Quality Assurance Engineer in Mansfield, Massachusetts, responsible for ensuring product design compliance with regulatory and quality requirements.... ...and 2-5 years of experience in medical device quality or design assurance. Excellent analytical...Suggested
$23 - $30 per hour
...process. Quality Electronics Technician II Technical Mansfield, MA, US 6 days ago... ...will inspect, test, and troubleshoot the medical device products using assembly fixtures, work... ...documentation to ensure the product specification compliance. The Quality Electronics Technician is...SuggestedHourly payWork experience placement$65k - $85k
Corin Group in Raynham, MA is hiring a Quality Engineer to provide quality leadership in compliance with FDA and ISO regulations. The role includes establishing... ...with extensive knowledge of quality systems for medical devices. A base salary range of $65-85k is offered along...Suggested- 6029-MEDICAL DEVICE BUSINESS SERVICES, INC. is seeking a Senior Quality Engineer in Raynham, MA. The role involves leading quality assurance at various contract manufacturing... ...quality improvement initiatives, ensuring compliance with quality standards, and conducting audits...SuggestedContract work
$45k
...alert: Business Unit: Advanced Medical Components Posting Date: Mar... ...and materials Ensure compliance to federal and state laws, as... ...such as but not limited to, Engineering, when required EDUCATION and/... ...Experience working in medical device manufacturing Knowledge and experience...Hourly payWork at officeLocal area$87.4k - $131k
...Position Summary The Quality Assurance Engineer shall support the facility and departments... ...maintain thorough documentation for compliance. Monitor key performance indicators (KPIs... ...Assurance experience working in the medical device manufacturing environment (a combination...Temporary workFlexible hours- NextPhase Medical Devices LLC is seeking a Quality Electronics Technician II in Mansfield, MA. This role involves ensuring product quality through inspection and testing of medical device products. Applicants should have experience in regulated manufacturing environments...
- ...Summary and Objective: The Mechanical Engineer II will collaborate with team members to design and refine cutting-edge medical devices, contributing to product testing,... ...product feasibility and design, ensuring compliance with client and industry specifications....Temporary workWork experience placementWork at office
$87.4k - $131.1k
...Design Quality Assurance (DQA) Engineer is responsible for ensuring... ...Management to ensure design control compliance, effective risk management,... ...documentation. Review Device Master Record (DMR) elements... ...Minimum 2-5 years of experience in medical device quality or design...Temporary workFlexible hours$74.25k - $111.5k
...Plastics Injection Molding - Manufacturing Engineer II (US - Mansfield)Applylocations:... ...processing and mold maintenance to support medical device production. This role requires a... ...and process deviations.* **Validation & Compliance (GMP/ISO):** Develop and execute validations...Flexible hours- Quality Systems Specialist II - Training processes and Learning Management System (LMS) Contract Client is a Medical Device company. Implementation of the training process and... ...duties as assigned. Perform duties in compliance with environmental, health and safety related...Contract work
$90k - $125k
...application process. Quality Engineer Professional Mansfield, MA, US... ...System (QMS) to ensure compliance to FDA Quality System Regulation... ...quality assurance support to medical device development and validation efforts... ...requirements for Class I, II and III medical devices. In-depth...Work at office$71.3k - $97.75k
...set new standards of care. The Process Engineer II is responsible to understand, optimize... .... They execute of their duties in compliance with corporate policies, U.S. Food and... ...9001, ISO 13485, EU MDR, the Canadian Medical Device Regulations (CMDR), and other applicable...Full timeTemporary work$81.65k - $112.7k
Integra LifeSciences Corporation is seeking a Senior Engineer, Quality Design Assurance, to drive the development of medical devices. This role involves collaboration with R&D, conducting risk analyses, and ensuring compliance with regulatory standards. With a focus on...$74.25k - $111.5k
Smith & Nephew is seeking a Manufacturing Quality Engineer II in Mansfield, MA. This role involves improving product and process quality in a fast-paced manufacturing environment. You will lead investigations, apply statistical analysis, and develop inspection strategies...- Smith & Nephew is seeking a packaging engineer based in Mansfield, Massachusetts. The role involves designing and developing sterile... ...in Packaging Engineering, with significant experience in the medical-device sector. Qualified candidates will collaborate with various...
- ...development teams and must be knowledgeable in FDA regulations and medical device submissions. This role involves providing regulatory assessments, collaborating with international teams, and ensuring compliance with related standards. Applicants who meet the qualifications...
- ...Manager for a remote opportunity. The role involves ensuring compliance with FDA regulations, leading regulatory submission processes... ...Candidates need a Bachelor’s degree, 5+ years of experience in medical device regulatory affairs, and strong leadership skills. This...Remote job
$96.75k - $145k
...cross-functional teams, overseeing the scaling of innovative medical technologies. The ideal candidate will have 8+ years of experience... ...in regulated industries and significant knowledge of medical device compliance. This role offers a competitive base compensation ranging...- KLA-Belgium in Westwood, MA is seeking an Associate Test Engineer II to support assembly and testing of precision electro-mechanical systems. This role requires strong technical skills and offers a pathway to increased system-level ownership. The ideal candidate has a technical...
- ...professional for a role in regulatory affairs. The candidate will be responsible for preparing and auditing medical device DHFs and risk management files while ensuring compliance with US and international regulations. The ideal applicant should have hands-on experience in...
- ...experienced Regulatory Affairs Manager to ensure compliance with FDA and other regulations for medical devices. This role requires a minimum of 5 years in regulatory... ...possess a Bachelor's degree in a scientific or engineering field and have a solid understanding of...Permanent employment
- ...Regulatory Affairs contracted professional with experience working on product development teams, familiarity with FDA regulations for medical devices, submission experience of 510(k)s, generation of files necessary for outside U.S. notification and registration of medical...
- Integra LifeSciences is seeking a Quality Compliance Manager for their Mansfield, MA site. This role involves overseeing the implementation... ...Bachelor's degree, 10+ years of leadership experience in the medical device industry, and strong communication skills. This position...
$90k - $125k
NextPhase Medical Devices LLC is seeking a Quality Engineer in Mansfield, MA. The role involves ensuring compliance with FDA regulations and ISO standards while supporting product development efforts. Ideal candidates will have a Bachelor's in Engineering or Quality Assurance...- ...Regulatory Affairs Manager ensures compliance to FDA and other applicable... ...FDA submissions which may include device 510(k), IDEs, PMAs) and serving as... ...s degree required. Scientific or engineering field preferred. 5+ years of medical device regulatory affairs experience...Permanent employmentLocal area
- ...alta Technologies (RT) is looking for a Process Engineer to lead process engineering activities for a medical device client in Raynham, MA. The ideal candidate will... ...for driving process improvements, ensuring compliance with regulatory requirements, and supporting new...
$84k - $134.1k
...programmable logic controllers.Maintaining and sustaining a culture of compliance both in how we design solutions and in how we run and... ...Need (Basic Qualifications)*** Bachelor of Science degree in Engineering, Computer Science, or a related technology discipline.* 2-3...Permanent employmentFull timeApprenticeshipWork at officeWorldwideShift work- ...automation strategy for advanced manufacturing systems in Norwood, MA. This involves driving innovation in process automation, ensuring compliance with regulations, and managing complex projects. The ideal candidate has extensive experience in Pharma/Biotech systems, a strong...
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