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The ideal candidate will have a BS degree in Engineering and over 5 years of experience in Systems Engineering, particularly in medical device development. MillenniumSoft Inc is seeking a Systems Engineer III in San Diego, CA to lead technical excellence in product development.
This role focuses on supporting high-quality production of medical devices while ensuring compliance with regulations. Internetwork Expert is seeking a Quality Engineer to join their team in Carlsbad, California. A Bachelor’s degree in engineering and 3+ years experience in quality engineering or
This contract position will focus on leading and supporting initiatives in design and development, ensuring thorough verification and validation of systems.
A leading company in the workforce solutions sector is seeking a Product Assurance Analyst to manage and investigate product quality complaints. This role requires a customer-focused individual with strong analytical skills, knowledge of regulatory compliance, and the ability to work closely with cr
Senior Quality Engineer – Design Assurance (Firmware / Electrical Systems). Quality Engineering, Design Assurance, Product Quality, or related experience. Class III medical devices, implantables, cardiac rhythm management, pacemakers, or neuromodulation.
A leading biotech company in California seeks a Senior Quality Engineer to enhance their Quality Management System towards ISO 13485 compliance. This role requires a minimum of 5 years' experience in the medical devices field and expertise in Risk Management, Verification, and Validation.
Job Overview – Design Quality Engineer (Medical Devices) Compensation: $130,000 – $155,000/year + bonus Location: San Diego, CA Schedule: Monday to Friday (Hybrid) Atlantic Group is hiring a Design Quality Engineer (Medical Devices) in San Diego, CA for our client, supporting software quality
Candidates should have a bachelor's degree and significant experience in Agile PLM and medical device quality management systems. The role supports, configures and optimizes Oracle Fusion Cloud PLM within a regulated medical device environment, ensuring compliance with FDA and ISO standards. Respons
The role involves implementing hardware design processes and ensuring compliance with regulatory standards within the medical device industry. A leading technology firm seeks a highly skilled Hardware Quality Engineer for a remote position.
You will maintain quality management systems, support audits, and ensure regulatory compliance. Werfen in San Diego is looking for a Staff Quality Engineer to ensure compliance and excellence in IVD and medical device products. In this individual-contributor role, you will collaborate with R&D and M
The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals. Coordinate governance proc
The ideal candidate will advise on company clinical quality strategy, ensure compliance to regulations, oversee quality management systems and interact directly with cross functional clinical, regulatory and quality teams. Provide strategic and operational leadership in the planning and executing of
Supplier Quality Engineer in San Diego to enhance supplier quality and drive innovation in healthcare. The role involves addressing supplier quality issues, improving oversight processes, and collaborating with teams on compliant supplier management.
We are seeking an experienced Project Manager to lead a cross-functional medical device development program covering firmware updates, PC software development, hardware qualification, and manufacturing release. Proven experience managing projects in regulated environments (medical devices, healthcar
Project Manager Embedded Systems & Medical Devices. We are seeking an experienced Project Manager to lead a cross-functional medical device development program covering firmware updates, PC software development, hardware qualification, and manufacturing release. Proven experience managing projects
The Senior Manager, Quality Assurance GCP will support the Good Clinical Practice (GCP) Quality Assurance (QA) function, and performance of GCP QA operations. This individual will manage and oversee assigned audits, support regulatory inspections, and support the quality oversight and compliance pro
Regulatory Affairs, Licensing and Accreditation Supports multi?hospital regulatory readiness and ongoing compliance with Joint Commission, CDPH, CMS, and other applicable regulatory and accreditation agencies. The position supports operational planning and development of multi?hospital performance i
The Director of Digital Systems Quality Assurance (DSQA) is responsible for establishing, leading, and continuously improving the quality oversight of GxP digital systems supporting gene therapy manufacturing, pharmaceutical development, and analytical laboratories. Role-related knowledge: Working k
Project Manager Embedded Systems & Medical Devices. Hands-on experience working under formal design control processes and quality systems. Proven experience managing projects in regulated environments (medical devices, healthcare, or similar).