QA Specialist - Regulated Medical Devices & Compliance
W. L. Gore & Associates, Inc.
W. L. Gore & Associates, Inc. is seeking a Quality Assurance Professional to join Gore Medical Quality Assurance in Phoenix. You'll work with cross-functional teams to support day-to-day manufacturing, execute NCR, CAPA, Change Management, and other quality system processes, and implement corrective actions. The role is located at our Phoenix facility with a hybrid work arrangement. You will monitor post-implementation effectiveness and ensure audit readiness, collaborating across product lines #J-18808-Ljbffr W. L. Gore & Associates, Inc.
- W. L. Gore & Associates in Phoenix, AZ is seeking a Quality Assurance Professional to join the Gore Medical QA team. You will support day-to-day manufacturing, execute NCR, CAPA, Change Management, and other quality system processes, addressing product issues and implementing...Medical device
- ...candidate will have a Bachelor’s degree in engineering and at least 2 years of experience in the medical device industry. This role involves ensuring compliance with regulations, managing inspections, and maintaining product traceability. Benefits include competitive...Medical deviceFlexible hours
$102k - $109k
...you passionate about quality, compliance, and building trusted... ...ensure compliance with industry regulations and McKesson quality standards... ...company matching contributions Medical, dental, and vision benefits... ...environment, including medical device, pharmaceutical, supplier qualification...Medical deviceContract workWork at officeWork from homeHome office- ...of regulatory documents for medical device and IVD products. This role... ...projects, ensuring compliance with FDA, ISO 13485, and other... ...85, IVDR, and other global regulations, communicating relevant updates... ...mentorship to junior staff or specialists on assigned project...Medical deviceWork at office
- ...Hire A DAY IN THE LIFE OF the Director Medical Device Manufacturing Operations We’re building... ...-to-day operations. All within an FDA-regulated environment. It’s a high‑visibility opportunity... ...and ensuring ongoing FDA/ISO compliance. REQUIREMENTS Bachelor’s degree in Engineering...Medical deviceFull timeH1bVisa sponsorshipWork visaMonday to Friday
- ...quality of clinical research activities. This role requires implementing a Quality Management System and ensuring compliance with standards and regulations. The ideal candidate will have an associate degree and a minimum of 2 years of experience in clinical quality assurance...Full time
- ...continuously improve clinical safety processes for LDT and medical device studies in a regulated healthcare environment. You will lead safety planning,... ...assessments, and safety reporting, ensuring regulatory compliance. You will partner with cross-functional teams to align...Medical device
- ...Associate in Phoenix, AZ. The role involves supporting the Clinical Research Department's quality operations while ensuring compliance with regulations and maintaining research integrity. The ideal candidate will have an associate degree, 2+ years in clinical quality...Full timeWork at office
- ...leader to oversee manufacturing, planning, purchasing, materials, and distribution in a regulated medical device environment. The role balances quality, delivery, cost and compliance while guiding strategic planning and multi-area operations. The position emphasizes...Medical device
- Gore seeks a Quality Assurance Professional to join its Gore Medical Quality Assurance team in Phoenix, Arizona. You will support day-to-day manufacturing and plant operations, including NCR, CAPA, Change Management, and other quality system processes, addressing product...Medical device
$77.7k - $129.5k
...Senior Medical Packaging EngineerJoin a role focused on developing... ...packaging systems for medical devices. This position contributes to... ...quality, performance, and compliance requirements.Work Flexibility... ...designing and testing packaging in a regulated...Medical device- ...strategic leader to oversee manufacturing operations in a regulated medical device environment. You will lead manufacturing, planning, purchasing... ...and distribution to balance quality, delivery, cost, and compliance, with broad scope across multiple operations. You will...Medical device
$135.6k - $225.9k
...leadership role overseeing manufacturing operations within a regulated medical device environment. This position is responsible for leading... ...distribution functions while balancing quality, delivery, cost, and compliance objectives. The role offers broad operational scope,...Medical deviceFull timeFor contractors- ...electronic health records electronic medical records interoperability medical devices telemedicine health... ..., and leading a small legal and compliance team. The ideal candidate will... ...experience, particularly in a highly regulated environment. Applicants for the...Medical deviceInterim role
$100k
...Reps and Clinical Sales Specialist contractors and works... ...instructions and regulations.Qualifications:Required... ...years' experience in medical sales Minimum of 3 years... ...competitors in the medical device arena Effective... ...increase workplace safety in compliance with the applicable...Medical deviceFull timeContract workFor contractorsLocal area- ...Regulatory Affairs Specialist III The Regulatory Affairs Specialist... ...documentation, standards compliance, and metrics development... ...ensure a consistent approach to regulations is adopted throughout the... ...affairs experience in medical device or pharmaceutical industry...Medical deviceWork experience placement
- ...seeking a Quality Assurance Quality Control Specialist to develop and maintain a system of... ...manufacturing and erection work, ensuring compliance with quality standards and driving... ...improvement. The ideal candidate has 2-3 years QA/QC experience in construction,...
- ...Management is seeking a Quality Assurance Quality Control Specialist to develop and maintain a robust QA/QC program for our cooling technology services,... ...inspections, and drive continuous improvement while ensuring compliance with codes and customer requirements. The role...
- Triumvirate Environmental, Inc. is seeking a QA/QC Specialist for the Casa Grande, AZ team to manage sampling and analysis of incoming materials and ensure profile compliance with regulatory permits. You will work closely with facility personnel, develop understanding of...
- ...seeking a Quality Assurance Quality Control Specialist to develop and maintain a system of... ...erection/installation projects, ensuring compliance with quality standards and fostering continuous... ...ideal candidate will have 2-3 years of QA/QC experience and a general...
- Cohere Beauty is seeking a Quality Assurance Specialist to build, uphold, and improve our Quality Systems. The role includes QA tasks, GMP compliance, audits, training, and documentation management onsite. This role covers entry to senior levels and involves collaborating...
- Triumvirate Environmental in Casa Grande, AZ is seeking a QA/QC Specialist to manage sampling and analysis of incoming materials, helping... ...validate facility acceptance criteria and regulatory permit compliance. You will work closely with facility personnel, applying attention...
- ...Senior Staff Medical WriterWork Flexibility: RemoteStryker is hiring a Senior... ...that supports global regulatory compliance and market access for medical devices. This position partners closely... ...4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device...Medical deviceRemote work
- ...established standards. Candidates are required to have an associate’s degree or equivalent experience and at least five years of relevant field experience in commercial construction. This role offers offers competitive benefits including medical and 401(k). #J-18808-Ljbffr CBREFor subcontractor
- ...Assurance Professional to join the Gore Medical Quality Assurance team. In this... ...practices to ensure compliance Participate in and perform quality... ...related experience in a medical-device, pharmaceutical, biotech or other regulated industry Demonstrated working knowledge...Medical deviceVisa sponsorship
- ...retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial... ...multiple concurrent projects and initiatives involving IT, compliance, operations, and business stakeholders. Collaborate with project...Medical deviceRemote jobH1bVisa sponsorship
$130.5k - $363.5k
..., expense reporting, and other required documentation.Ensure compliance with promotional program requirements, proper use of promotional... ...sales experience within the pharmaceutical, biotechnology, medical device, or healthcare industry.Minimum of 5 years of oncology sales...Medical deviceFull timePart timeLocal areaImmediate startWorldwide- ...preferred, or demonstrated equivalent experience supporting medical device regulatory activities Minimum of 1 year of experience in medical... ...device regulatory affairs, clinical research, or related regulated industry required Familiarity with medical device product development...Medical deviceFull timeH1bWork at officeVisa sponsorshipWork visaMonday to FridayFlexible hours
- ...VASCULAR SALES SPECIALIST For more than 20 years, BioTAB... ...compression devices and personalized service... ...Knowledge of healthcare regulations and insurance... ...relationships with VA medical staff, specialty civilian... ...progress and ensure compliance with treatment protocols...Medical deviceFull timeContract work
- TileBar in Tolleson, AZ is seeking a Quality Assurance Specialist to ensure warehouse products meet quality standards from receipt to shipment. You will audit processes, maintain records, and collaborate with leaders to implement corrective actions. The role requires attention...
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