- Gilead Sciences, Inc. (Santa Monica, CA)
- …aspirations. Join Gilead and help create possible, together. **Job Description** **Sr Manager , SAP CGTO Solutions Architect** **Job Overview:** We are seeking an ... CGTO & SAP SD, MM & PP modules, regulatory compliance (such as GxP and FDA ), and life sciences Quality Management and Batch Release processes. As an SAP CGTO… more
- Gilead Sciences, Inc. (Foster City, CA)
- …expertise in SAP BRH & SAP QM module, regulatory compliance (such as GxP and FDA ), and life sciences Quality Management and Batch Release processes. As an SAP BRH ... S/4HANA and other related systems (QMS, LIMS etc.,) and driving business process excellence in a regulated environment. This role involves strategic oversight and… more
- Keurig Dr Pepper (Sacramento, CA)
- **Job Overview:** The QEHS Manager is accountable for the Quality and Environmental, Health and Safety Program at the site. Direct report to the Plant Director, the ... QEHS Manager provides site leadership in Food Safety, Quality Assurance,...six sigma Quality performance, and 100% compliance to all FDA , EPA and OSHA regulations. **Location:** This position is… more
- Sumitomo Pharma (Sacramento, CA)
- …a dynamic, highly motivated, and experienced individual for the position of Senior Manager , Regulatory Operations, For assigned projects, the Senior Manager of ... publishing, distribution, and archiving of health authority submissions. The Senior Manager will oversee the activities of external publishing staff contracted to… more
- Terumo Neuro (Aliso Viejo, CA)
- **12521BR** **Title:** Sr. Manager , Clinical Data Management **Job Description:** The Senior Manager , CDM oversees clinical data management activities across ... accurate, high quality clinical data and adhering to Good Clinical Practices and FDA regulations. Job duties: + Develop and implement SOPs to ensure GCP/ICH… more
- Kelly Services (Valencia, CA)
- + **Regulatory Affairs Manager ** + **Location:** Onsite in Valencia & Burbank, CA + **Salary:** $100,000-$140,000/year (DOE) + **Industry:** Medical Device / Life ... Kelly(R) Science & Clinical is hiring a **Regulatory Affairs Manager ** for a leading client. In this role, you'll...leading client. In this role, you'll ensure compliance with FDA , ISO, and international regulations and submissions while managing… more
- Charles River Laboratories (Northridge, CA)
- …Solutions, you will make a difference every day. **Job Summary** Project Manager I will coordinate both internal operations projects and client-facing programs in ... projects simultaneously. Experience in client communication, regulatory environments, and process improvement is highly desirable. Essential Responsibilities + Lead… more
- Abbott (Alameda, CA)
- …114,000 colleagues serve people in more than 160 countries. **Sr. Software QA Manager (Non-Product)** **Working at Abbott** At Abbott, you can do work that matters, ... and Abbott corporate requirements. (Such as, ISO 13485 and FDA 21 CFR part 820, and IVD/MDD directives). Will...non-product software quality team reporting directly to the SWQA manager . + This is a senior level position with… more
- Abbott (Alameda, CA)
- …with our new sensing technology. **The Opportunity** This **Regulatory Affairs Manager - International Compliance Operations** will work on-site at our Alameda, ... glucose levels with our new sensing technology. This **Regulatory Affairs Manager - International Compliance Operations** will provide support for the regulatory… more
- Compass Group, North America (San Fernando, CA)
- …your journey with us today! Job Summary Job Summary: The Quality Assurance Manager is responsible for development and maintenance of all QA programs, meeting USDA, ... FDA and customer requirements and ensuring the quality and...requirements. + Must have extensive knowledge of the facilities process flow and engage personnel in all areas of… more