- Herbalife (Lake Forest, CA)
- Specialist, Document (Technical Operations) Category: Manufacturing Position Type: Regular Full-Time External ID: 18478 Location: Lake Forest, CA, United States Date ... on LinkedIn share to linkedin Apply Now **Overview** **THE ROLE:** The Document Specialist, Technical Services will primarily be responsible for maintaining and… more
- Astrix Technology (Los Angeles, CA)
- **QA Document Control Specialist** Clinical Pharmacology Los Angeles, CA, US + Added - 27/08/2025 Apply for Job _Our client has over 50 years of experience and ... offers a comprehensive range of services._ **Title:** Quality Assurance Document Control Specialist(Contract) **Location:** Fully Onsite - Torrance, CA **Schedule:**… more
- LinkedIn (Mountain View, CA)
- … regulatory changes impacting LinkedIn. + Support internal and external audits, regulatory inquiries, and enforcement actions + Support management in handling ... practical experience. + 4+ years of experience in risk management , regulatory compliance, or audit. + Demonstrated...Candidates ** Please follow this link to access the document that provides transparency around the way in which… more
- Ascendis Pharma (Palo Alto, CA)
- …The Regulatory Project Manager will be an integral part of Global Regulatory Affairs, providing project management leadership to key global regulatory ... across regions to ensure the delivery of business objectives. + Participate in Regulatory filing teams, providing project management expertise in the end-to-end… more
- Kelly Services (South San Francisco, CA)
- …with company procedures. + Take initiative in resolving minor issues related to document management and training. + Recommend and implement methods to increase ... ** Document Control Specialist** Kelly(R) Science & Clinical is...of GMP documentation and training records within the Quality Management System (QMS), directly contributing to the advancement of… more
- Deloitte (Sacramento, CA)
- …information and respond to regulatory or litigation requests. + Performs document management and review functions such as reviewing files, preparing indexes, ... service of process. + Inputs data, maintains and updates OGC's litigation matter management system and its service of process tracking database. + Circulates copies… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …annual budget, and manage spend. + Author and conduct periodic review of regulatory intelligence management Standard Operating Procedures or work practices. + ... The Associate Director of Regulatory Intelligence leads the collection and dissemination of...platform. + Lead internal process to obtain, coordinate, and document cross-functional SME impact assessments of new or updated… more
- Sumitomo Pharma (Sacramento, CA)
- … strategies and the ability to contribute to the development and writing of a regulatory strategy document + Ability to make complex decisions and willingness to ... highly motivated, and experienced individual for the position of **Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part of the Global … more
- Terumo Neuro (Aliso Viejo, CA)
- …with regulatory agencies on administrative and routine matters. + Document , consolidate, and maintain verbal and written communication with the regulatory ... **12814BR** **Title:** Associate Principal, Regulatory Affairs **Job Description:** Responsible for establishing and preparing strategy for worldwide product… more
- Sumitomo Pharma (Sacramento, CA)
- …will be responsible for leading development of all non-clinical and clinical regulatory strategies including management of IND and NDA submissions, FDA ... activities; provide relevant input to Leadership + Oversee the regulatory activities at CROs, providing document review...Oversee the regulatory activities at CROs, providing document review in order to ensure the quality and… more