- Sharp HealthCare (San Diego, CA)
- …**Shift** Day **FTE** 1 **Shift Start Time** **Shift End Time** California Clinical Microbiologist Scientist License - CA Department of Public Health; Bachelor's ... Degree; California Clinical Toxicologist Scientist License - CA Department of Public...conditions or situations that may be or are compromising quality of care.Supports and provides input for development, revisions,… more
- Abbott (Santa Clara, CA)
- …analysis for regulatory compliance. **Premarket:** + Assess the acceptability of quality , preclinical and clinical documentation for submission filing. + ... software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an onsite opportunity working out of our Santa Clara,… more
- J&J Family of Companies (Santa Clara, CA)
- …CFR, regulatory agency guidance documents) + Review and approve R&D, quality , preclinical and clinical documentation for submission filing + In collaboration ... America **Job Description:** Johnson & Johnson is hiring for a **Senior Regulatory Affairs Specialist (Remote) - Shockwave** to join our team. This is a remote role… more
- Kestra Medical Technologies, Inc (Escondido, CA)
- …modern wearable technologies with proven device therapies. Kestra's solutions combine high quality and technical performance with a wearable design that provides the ... harmoniously monitor, manage, and protect life. The ASSURE Patient Specialist (APS) conducts patient fitting activities in support of...of the sales organization and the team of Regional Clinical Advisors (RCA). The APS will serve as the… more
- Boehringer Ingelheim (Fremont, CA)
- …manufacturing organizations (CMOs) and contract laboratory organizations (CLOs). The Senior Specialist , Supplier Quality Management (SQM) will execute SOPs and ... **Description** The **Sr Specialist , SQM** role offers a base salary typically...of the supplier life cycle (eg, audits). + Generation, review , negotiation and maintenance of Quality Assurance… more
- Medtronic (Irvine, CA)
- …projects and prioritize tasks to meet project schedules + Interface with engineering, quality , clinical , marketing, and other functions as needed to fulfill ... **A Day in the Life** The Sr Regulatory Affairs Specialist will play a key role in sustaining the...on the project team throughout the product lifecycle. + Review promotional and advertising material + Maintain current regulatory… more
- Veterans Affairs, Veterans Health Administration (San Diego, CA)
- …Coordinating with Service Chiefs and service level administrative teams for annual Committee(s) review of clinical privileges and scope of practice. Serving as ... Summary The Supervisory Health System Specialist - Credentialing and Privileging Manager position is...reviews and assessments, privileging actions, and guidance related to clinical performance concerns. Responsible for ensuring quality … more
- Envista Holdings Corporation (Brea, CA)
- …CE technical files in accordance with applicable regulatory requirements. + Author, review , and approve Clinical Evaluation Reports (CER), Summary of Safety ... **Job Description:** The **Regulatory Affairs Specialist ** creates, evaluates and completes regulatory tasks related to worldwide product registration submissions,… more
- Datavant (Sacramento, CA)
- …to realize our bold vision for healthcare. **What We're Looking For:** As a Clinical Documentation Quality Improvement (CDQI) Specialist , you will play a ... to enhance documentation clarity, completeness, and overall medical record quality . By ensuring accurate and comprehensive physician documentation, you will… more
- Bayer (Berkeley, CA)
- …minds to make a real difference, there's only one choice.** **Senior Specialist , Conformance** **PURPOSE:** The Senior Specialist , Conformance is a senior ... investigating and resolving higher category discrepancies that occur in clinical and commercial biological manufacturing operations. **YOUR TASKS AND… more