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Coordinate and collaborate regulatory activities across functions within ORIC, ie, regulatory operations, quality, CMC, nonclinical, clinical. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals, and in compliance with all applicable regulatory requiremen
ORIC Pharmaceuticals is looking for a Director/Associate Director of Regulatory Affairs in San Diego. The role involves leading regulatory submission efforts and collaborating with cross-functional teams to ensure compliance and quality in submissions. The ideal candidate will have over 8 years of r
This full-time position involves supporting and leading regulatory activities for oncology products and ensuring compliance with global regulatory requirements. The ideal candidate has a Bachelor’s degree and 8+ years in regulatory affairs, with strong communication and organizational abilities. D
Coordinate and collaborate regulatory activities across functions within ORIC, ie, regulatory operations, quality, CMC, nonclinical, clinical. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals, and in compliance with all applicable regulatory requiremen
Medical Billing Specialist (Revenue Cycle Management) – Bilingual Spanish Preferred. Multi-location healthcare billing experience. Medical Billing Specialist with demonstrated.
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.
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
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.
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.
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
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
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 contract position will focus on leading and supporting initiatives in design and development, ensuring thorough verification and validation of systems.
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
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
Proven experience managing projects in regulated environments (medical devices, healthcare, or similar). 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). Hands-on experience working under formal design control processes and quality systems. Technical awareness of embedded systems, firmware (ARM/C), PC applications (C/C++/C#), and hardware-software
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. Years experience in performance improvement, quality, patient safety, regulatory affairs,
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.
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. Support Global Regulatory