- Gilead Sciences, Inc. (Foster City, CA)
- …accelerate development and approval timelines. Provide guidance to PDM Teams and Device Teams to align development and regulatory path for combination products and ... Cultivate strong, collaborative relationships across Gilead's global functions, including Quality , Manufacturing, Technical Development, Clinical Development, and Supply Chain.… more
- Abbott (Pleasanton, CA)
- …levels in the organization. + Minimum of ten (10) years' experience in medical device development and/or other highly regulated industry + Previous experience ... with quality . You will work closely with cross-functional peers in quality , operation, marketing, clinical and regulatory, medical affairs, commercials to… more
- United Therapeutics (Sacramento, CA)
- …), livers ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)** ), with plans ... of biologic or pharma regulatory experience with a Bachelor's Degree in life sciences, quality , regulatory affairs or a related area of study or 10+ years of… more
- Edwards Lifesciences (Los Angeles, CA)
- …including expert understanding of US GAAP and SEC reporting standards + Medical Device industry experience highly preferred + International entity exposure ... play a fundamental role in how we impact the quality of life for patients all over the world....for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination… more
- Edwards Lifesciences (Irvine, CA)
- …assigned studies + Contributing to additional initiatives that shape the future of medical device development **What you'll need (Required):** + Ph.D. or ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- NTT America, Inc. (Santa Clara, CA)
- …ensuring they are completed on time, within budget, and to the highest quality standards. + **Stakeholder Collaboration** : Work closely with internal and external ... expenses associated with working remotely and use of a personal mobile device , if applicable._ NTT Global Data Centers Americas, Inc. offers competitive compensation… more
- J&J Family of Companies (Santa Clara, CA)
- … or above in a quality function across Design and Development including End-to-End Quality & Compliance in Medical Device . + Must have a minimum of ... on effective, reliable, agile, compliant and scalable QMS. **Sr. Director , Quality & Compliance; Monarch Platform will:**...5 years of large-scale Capital Medical Device Equipment experience as a quality leader… more
- Hologic (San Diego, CA)
- …Auditing or similar roles + Clean driver's license + Proficient knowledge of Medical Device Regulations, In Vitro Diagnostic Regulation, cGMP, CFR 820, ... part of our mission to deliver safe and effective medical devices that enhance patient outcomes. **Key Responsibilities** +...quality or regulatory issues to the Global Supplier Quality Sr. Director / Director that may… more
- BD (Becton, Dickinson and Company) (Brea, CA)
- …devices marketed in all regions throughout the world. + Expertise in failure investigation and medical device CAPA process. + Experience in medical device ... **Job Description Summary** Sr Design Quality Systems Manager reports to the Director...working in a design center. **Knowledge and Skills:** + Quality Management Systems requirements for medical devices… more
- Aerotek (Santa Rosa, CA)
- …and compliant with internal and external standards, working closely with the Quality Director . **Responsibilities** + Manage and maintain all quality ... data analysis. + Experience with auditing tools and software. + Background in the medical device industry is beneficial. **Why Work Here?** Relucent offers a… more