- Meta (Menlo Park, CA)
- … fraud & abuse. **Required Skills:** Associate General Counsel, People, Planet, Device Compliance Responsibilities: 1. Assist in the design and implementation ... 6. and healthcare fraud & abuse. 7. Develop and communicate compliance policies, processes and training. 8. Manage and conduct internal compliance … more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... and 5+ years of related experience performing Quality System related activities in the medical device industry. + Working knowledge of cGMP, FDA 820 QSR and… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... and partners with internal/external departments to efficiently deliver safe and effective medical device designs for manufacturing, which are in line with… more
- GRAIL (Menlo Park, CA)
- …counsel. + 20+ years of Compliance and Privacy experience in in-house medical device , biotech, clinical laboratory, pharmaceutical, or other life sciences or ... & HCOs: provide strategic counseling guidance across Commercial and Medical on interactions with HCPs & HCOs, including procedures,... issues and related policies and procedures. + Global Healthcare Compliance : update GRAIL policies to address… more
- Abbott (Pleasanton, CA)
- …field + Eight (8) years of Quality Systems, Quality Assurance and/or Regulatory Compliance /Affairs experience in medical device manufacturing or other ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...get on with their lives. As a Senior Quality Compliance Manager, the individual will play a crucial role… more
- Stryker (San Jose, CA)
- …minimum of 8+ years of work experience required . + 2-4 years experience in medical device with Bachelors or 1 year of experience with Masters degree, biologics ... Stryker is hiring **a Regulatory Operations Project Manager, Product Environmental Compliance ** . This position is **Remote** , supporting our **Endoscopy Division**… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... The Principal Clinical Evaluation Specialist requires experience in the writing of medical device clinical regulatory documents. The position will mainly focus… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... complaint information. + Assist with training Customer and Shockwave Medical reps to ensure compliance to Shockwave...years of experience is highly preferred. + Experience with Medical Device Complaint handling, Post Market Surveillance… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...and ISO and ASTM standards related to quality and medical device industry is an asset. +… more
- Abbott (Alameda, CA)
- … Events Team provides direct supervision and management to staff responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000... Incident Reports to the EU/EFTA including France, and Medical Device Incident reports to the rest… more
- Abbott (Pleasanton, CA)
- …9+ years' experience in a Quality, Regulatory, or product development role in the medical device industry. + 5+ years' experience managing a team of ... regulations and guidance, ISO 13485, Software Standards (eg, IEC 62304), EU Medical Device Regulations, and MDSAP **Preferred Qualifications** Direct experience… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where... device pre- and/or post-market clinical studies + Medical Device experience is preferred + Ability… more
- US Tech Solutions (San Bruno, CA)
- …Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation ... the way people manage their health and the way healthcare is delivered. The purpose is to bring the...support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...market releases. + Product knowledge including product vigilance and medical device reporting. + High attention to… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...Minimum 5 years of regulatory affairs experience in the medical device industry with a Bachelor's degree;… more
- J&J Family of Companies (Santa Clara, CA)
- …leading in medical affairs, clinical development or related roles in research/ medical device industry is _strongly preferred_ . + 2+ years ... focus on Robotic Bronchoscopy. This role involves overseeing clinical research, ensuring compliance with medical regulations, supporting medical safety, and… more
- Abbott (Alameda, CA)
- …technical, manufacturing, quality, or supply chain experience in a health care/ medical device company + Excellent interpersonal skills and demonstrated ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...experience + Minimum 5 years working in a regulated medical (ideally device or in vitro Diagnostic)… more
- Abbott (Alameda, CA)
- …years Quality Assurance, Technical Quality, or equivalent + Minimum 3 years medical device manufacturing industry **Preferred Qualifications** + Some Knowledge ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...QSR and ISO regulations + Knowledge and experience with medical device regulations for device … more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... to mitigate risks associated with commercial transactions and agreements within the medical technology industry. ** Compliance :** Stay abreast of evolving laws,… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...medical or other technical fields and Class III medical device experience are preferred. + Ability… more