- Stryker (San Jose, CA)
- …support our Endoscopy division. In this role, you will lead the development, review , and approval of sterilization processes and equipment validations (IQ, OQ, PQ) ... sterilization, and biocompatibility for reusable medical device design. + Develop, review , and approve sterilization processes and equipment validations (IQ, OQ,… more
- Abbott (Sylmar, CA)
- …remediation plans and corrective actions. + Assists in facilitating the routing for review of new and/or updated divisional policies, procedures and related forms. + ... + Assists with the preparing for, scheduling, and follow-up from Compliance Review Committee meetings. + Coordinates compliance Review Committee meetings.… more
- Cordis (Santa Clara, CA)
- …quality standards and regulations. + Collaborate with cross-functional teams to create, review and approve manufacturing documents. + Conduct root cause analysis and ... in the preparation and reporting of quality metrics during operations and quality review presentations at defined intervals. + Review and approve complaint,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Provide scientific and clinical leadership or oversight in the preparation, review , and interpretation of clinical study data, ensuring high quality data + ... safety monitoring, and ensuring high data quality through data review as part of a cross-functional team + Lead...for one or more projects + Thorough understanding of pharmaceutical regulatory requirements and impact on development and execution… more
- Bristol Myers Squibb (San Diego, CA)
- …following. Other duties may be assigned. + Oversee vendors' activities, and review vendors' deliverables to ensure quality + Create/QC SDTM/ADaM data specifications, ... internal ad-hoc requests + Collaborate with cross-functional teams to review critical study documents and perform data reviews for...or equivalent with at least 10 years' experience in pharmaceutical industry; or a master's degree in statistics or… more
- BeOne Medicines (Emeryville, CA)
- …Functions of the Job:** + Facilitate generation of, author, update, and/or review key documents, including, but not limited to: + Protocol concepts, synopses, ... respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CROs + Review , query, and analyze clinical trial data + Interpret, and present clinical… more
- BeOne Medicines (San Carlos, CA)
- …and bio-sample testing activities for clinical trials, including but not limited to review and finalize lab vendors key documents (such as lab manual, lab database ... activities and initiatives. + Collaborate with internal teams to review key study documents such as ICF, EDC design...MD, PHD in biology/medical major. + Experience in the pharmaceutical industry and/or academia is preferred + Understanding of… more
- Mentor Technical Group (Redwood City, CA)
- …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... and corrective maintenance in the most effective and efficient way. + Review and approve/disapprove incoming work requests. + Develop and report work backlog… more
- BeOne Medicines (San Mateo, CA)
- …Functions of the job: + Facilitate generation of, author, update, and/or review key documents, including, but not limited to: + Protocol concepts, synopses, ... respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO's * Review , query, and analyze clinical trial data + Interpret, and present clinical… more
- J&J Family of Companies (San Francisco, CA)
- …+ Health Sciences + Kinesiology + Informatics and/or Data Science + Pharmaceutical Science + Physics + Technical Design: Industrial Design/Product Design + A ... and respectful of your time. Here's what you can expect: * Application review : We'll carefully review your CV to see how your skills and experience align with… more