QA Release Lead for Regulated Medical Devices
$95.5k - $126.3kIBA Worldwide
A leading medical technology company in Idaho is seeking a QA Product Release Associate to ensure compliance and quality for its life-saving proton therapy products. The ideal candidate has a strong background in quality assurance within regulated environments. This role includes responsibilities such as approving product releases and conducting quality reviews. The position offers a salary range of $95,500 to $126,300 along with comprehensive benefits. #J-18808-Ljbffr IBA Worldwide
$140k - $180k
...Global Quality Assurance to oversee manufacturing and product release activities. This role demands extensive experience in the pharmaceutical... ...Systems, ensuring compliance with regulatory standards, and leading teams across various quality-related activities. The position...SuggestedRemote job- Custom Processing Services Inc. is looking for a QA Technician to be the primary release agent for all production on the shift. The role involves reviewing data and documentation, performing internal audits, and supporting QC testing. The ideal candidate will have manufacturing...SuggestedWork at officeAll shifts
$95.5k - $126.3k
The QA Product Release Associate plays a critical role in ensuring the delivery... ...for the final release of devices, verifying compliance with... ...years of work experience in a regulated environment, in a quality... ...manufacturing or R&D environments for medical devices Working knowledge...Medical deviceTemporary workWork experience placementWorldwideFlexible hours- Role Summary bp is seeking a QA Lead - Test Automation Engineer to drive quality strategy... ...execution across multiple projects and releases. Design, develop, and maintain automated... ...utility, energy, oil & gas, or related regulated enterprise environments. Strong understanding...Suggested
$130k - $160k
...forward. As a global medical technology leader... ...a medical device design and manufacturing... ...Build, mentor, and lead a high-performing... ...quality control (QA/QC) team, fostering... ...ensure timely product release and market supply... ...ability applying regulations and standards...Medical deviceHourly payWork experience placementFlexible hours$140k - $180k
...receiving inspection and product release activities. As a quality... ...5 standards, FDA 21 CFR 820 regulations, customer requirements and... ...Responsibilities Responsible for , leading developing, implementing and... ...21 CFR 820 regulations for medical devices with a continuous...Medical deviceFull timeWork experience placementLocal areaShift work$140k - $180k
...Pharmaceuticals Inc. is a leading specialty... ...manufacturing and product release at the Medexus Contract... ...Pharmaceuticals for Human Use) regulations and guidances for Drugs, Biologics and Medical Devices. This position will lead... ...teams and provide QA review of technical manufacturing...Medical deviceContract workRemote work- ...Manager/Sr. Manager, GLP - CQA as part of the Regulatory Affairs team in Somerset, NJ. The role involves ensuring compliance with GLP regulations and maintaining a quality oversight system. The successful candidate will work with diverse teams to ensure inspection-readiness...
- A notable technology consulting firm in New Jersey is seeking a Sr. QA Lead Engineer to oversee quality assurance for software releases. This pivotal role involves managing a team of quality engineers, developing automation frameworks, and ensuring rigorous testing processes...
- ...maintain quality and regulatory systems in compliance with medical device regulations. This role involves collaborating with teams and managing supplier... ...have a BS or BA in a life science, possess 5-7 years of QA/RA experience, and be familiar with ISO and FDA requirements...Medical device
$120k - $200k
A leading tech company in New York City is seeking a QA Manager to oversee quality strategy across multiple products. The... ...testing efforts to ensure all releases are stable and compliant. Responsibilities... ...comprehensive benefits including medical coverage and generous PTO. #J-188...Work at office- Job Title: QA Lead/SME - Annuity Policy Administration Systems (ALIP, FAST, or any other Annuity Policy Admin product) Location: Holmdel... ...and review Master Test Plans, Phase‑wise Test Strategies, and Release Readiness criteria . Govern test execution across SIT, E2E,...Contract workH1bRemote workShift work
- ...not added on at the end. Our QA practitioners work alongside creative... ...‑based testing does not: device variance, platform behavior,... ...leave no margin for error. The QA Leads who thrive here understand... ...testing, ensuring stability across releases. Design test scenarios for...Immediate startRemote work
- ...compliance across juvenile correctional facilities. The role emphasizes adherence to federal regulations, agency standards, quality assurance audits, and expert consultation. You will lead QA tools, analyze procedures, prepare audit reports, support reaccreditation, and train...
- ...automation framework like Selenium. Establish and evolve formal QA processes, ensuring that the team is using industry-accepted best practices. Act as key point of contact for all QA aspects of releases, providing QA services and coordinating QA resources internally and...Work experience placement
- ...multiple jurisdictions, ensuring compliance with diverse and complex regulations. The Quality Assurance Regulatory Reporting Specialist will... ..., and the ability to operate effectively within a robust QA framework. Key Responsibilities: Quality Assurance Execution (Regulatory...Full timeWork experience placementLocal area
$100k - $160k
...manufactures, and markets hemostatic medical devices utilizing the company’s... ...Engineer is responsible for leading the design and development... ...to relevant Design Control regulations and standards. The person in... ...through product launch/release. Good working knowledge of...Medical deviceFull timeTemporary workPart timeApprenticeshipWork experience placementLocal area- ...opportunity for a Quality/System Engineer in the medical device industry. This role is crucial in... .... You will conduct gap assessments, lead design control processes, and maintain... ...engineering, and a strong understanding of regulations such as ISO 13485 and EU MDR. Join a...Medical device
$65k - $70k
...with Sales Representative(s) in the area to quickly learn the medical device industry and Upper Extremities business, and then contribute... ...adhering to applicable federal, state and local laws and regulations, accreditation and license requirements, and Company’s policies...Medical deviceFor contractorsLocal area- A leading medical device company is looking for a Supplier Quality Engineer to ensure compliance and quality in the supply chain for Class... ...audits. The ideal candidate should have experience in FDA regulations and a background in continuous improvement using Lean/Six...Medical device
- Position Description We are looking for an experienced QA Team Lead / QA Manager to lead and continuously improve our Quality Assurance function... ...throughout the software development lifecycle and that releases meet the highest standards before reaching clients. The position...Remote jobFull time
- ...Engineering and Land Surveying, D.P.C. is seeking a highly skilled Special Inspector in Westchester. You will oversee compliance with regulations on transportation and infrastructure projects, ensuring high quality and safety standards. The ideal candidate will have 5-7...
- Cloud Odyssey seeks a seasoned QA Lead for Salesforce Service Cloud projects. You will guide QA strategy, manage a team of analysts, and ensure testing coverage from design through release. The role emphasizes leadership, proactive issue mitigation, and clear communication...Remote job
- ...elements in conformity with domestic medical device agency regulations and requirements. Achieve quality assurance... ...similar with advanced experience in QA/RA areas or related training required... ...& Abilities Demonstrated success in leading and developing a collaborative team...Medical deviceWork experience placement
- A leading manufacturer of building products is seeking a skilled Release and Testing Coordinator to oversee software release processes and testing efforts. This role involves developing release plans, managing multiple testing phases, and collaborating with various teams...
$430k
...Comprehensive health benefits including Medical, Dental, and Vision Employee... ...work-life balance Chance to lead and shape a new sales... ...with medical sales regulations Foster a culture of integrity... ...experience within the Medical Devices or Neurostimulation industry...Medical deviceImmediate startFlexible hours- Framework Ventures is seeking a Compliance Training Coordinator to lead training sessions and ensure effective onboarding in the... ...strong analytical skills, and a solid understanding of BSA/AML regulations. The position offers competitive remuneration and a multinational...
- A leading manufacturer of Medical Devices in New York is seeking a Staff R&D Engineer. The R&D Engineer will lead the New Product Development process... ...mentor junior engineers, ensuring compliance with FDA regulations. Candidates should have a BS in Mechanical or...Medical device
- ...highly experienced Quality Assurance (QA) Manager to lead and oversee quality systems for our growing... ...products meet FDA dietary supplement regulations (21 CFR Part 111 and 117), labeling... ...). Complete and own finished product release and disposition decisions that do not...Contract workRemote work
- ...as software bill of materials, and software maintenance and release activities. Minimum Qualifications ~ Bachelor's... ...experience working with a quality system for Class III FDA-regulated medical devices. Skills and Knowledge In-depth knowledge of Design...Medical devicePermanent employmentTemporary workImmediate start
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