- Gilead Sciences, Inc. (Foster City, CA)
- …and launch submissions, as applicable. You may initiate and/or contribute to local process improvements for activities relating to the work of RA Ad/Promo. You may ... or therapeutic areas. + Maintains a continued awareness and understanding of FDA regulations, guidance documents, and enforcement actions with regards to advertising… more
- Edwards Lifesciences (Irvine, CA)
- …and central resource for all manufacturing plants and regional partners. * Process Champion for Inventory Forecasting, Inventory Entitlement Planning and Excess & ... to ensure yearly E&O target is met. * Identify process improvement opportunities and work with various owners on...guidelines relevant to local and/or global supply chain including FDA and ISO laws and regulations * Ability to… more
- Gilead Sciences, Inc. (Foster City, CA)
- …operations or clinical trial management experience. + Knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of ... Act of 1990, applicants who require accommodation in the job application process may contact ###@gilead.com for assistance. For more information about equal… more
- Danaher Corporation (West Sacramento, CA)
- …laboratory's role in improving healthcare outcomes. You will report to the Manager Technical Process Engineering, who is responsible for the Engineering ... tools that address the world's biggest health challenges As the Senior Process Engineer for Consumables Manufacturing at Beckman Coulter Diagnostics - Microbiology,… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …operations. The Manufacturing Specialist will work in conjunction with the Manager , Manufacturing to coordinate all logistics pertaining to manufacturing operations. ... this position will be responsible for assisting in document review and process trending. **ESSENTIAL DUTIES & RESPONSIBILITIES** include the following. Other duties… more
- Kelly Services (Sunnyvale, CA)
- …development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle ... Quality group in R&D and reports to the Sr. Manager , Product Lifecyle Quality and will be onsite based,...ensure continued compliance with internal procedures and applicable US FDA , EU IVDR, and other global standards. + Provide… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …a **maker of possible** with us. **Position Summary** The Senior Manager of EMI (Electromechanical Instruementation) Quality Sustaining Engineering reports to the ... at the EMI plant locations will report directly to the Senior Manager and are under their authority for performance reviews, career development, compensation,… more
- Stanford Health Care (Palo Alto, CA)
- …Ensures organizational compliance with federal/state regulations and accreditation requirements ( FDA , CDPH, BOP, TJC, etc.) for medication management. Develops audit ... Reviews, analyzes, and trends data to identify gaps and participates/leads process improvement activities. **Locations** Stanford Health Care **What you will do**… more
- Boehringer Ingelheim (Los Angeles, CA)
- …specialist role responsible for pull-through of the account plan (developed by the Account Manager ) at the Health System's various sites of care and with the Health ... + Uses approved account management techniques to facilitate the decision-making process and engagement. + Supports the Health Systems' Triple Aim efforts… more
- Medtronic (Irvine, CA)
- …if required. + Takes a leadership role in responding to relevant questions from FDA , FDA Advisory Panels, and/or other regulatory agencies, and in negotiations ... and analysis issues. + Lead development of policies and procedures for process improvements and standardization for the department and the statistics group. +… more