- Adecco US, Inc. (Swiftwater, PA)
- …local law; and Holiday pay upon meeting eligibility criteria Overview of the Position The Regulatory CMC Specialist will work closely with the Regulatory ... Adecco Healthcare & Life Sciences is hiring a contract hybrid Regulatory Affairs Specialist for... compliance for License registrations in existing markets. The Regulatory CMC Specialist in … more
- Merck (Rahway, NJ)
- …process & connectivity between functions supporting pipeline (ie clinical development, CMC , supply chain, & human health), and balancing needs of patients ... supplies. + Interacts with key partner organizations such as clinical development, regulatory , quality and other supply chain areas to address clinical supply… more
- West Pharmaceutical Services (Exton, PA)
- …ISO 14971, ISO 15223, IEC 62304, ISO 11608), 21 CFR Part 820 and CMC regulatory requirements. + Experience in medical device life-cycle Management, including ... Sr. Specialist , Regulatory Project Management (Evergreen Posting)...our careers website as follows:** **https://careers.westpharma.com/** **_This position is hybrid in Exton,PA. Candidates applying must be residing within… more
- LA Care Health Plan (Los Angeles, CA)
- Customer Solution Center Compliance Audit Specialist II Job Category: Customer Service Department: CSC Appeals & Grievances Location: Los Angeles, CA, US, 90017 ... achieve that purpose. Job Summary The Customer Solution Center (CSC) Audit Readiness Specialist II is responsible for the execution, oversight, and monitoring of the… more
- The City of Houston (Houston, TX)
- SENIOR COMMUNICATIONS SPECIALIST Print (https://www.governmentjobs.com/careers/houston/jobs/newprint/4713945) Apply SENIOR COMMUNICATIONS SPECIALIST Salary ... 1800 employees and is made up of Drinking Water Operations, Planning, Regulatory Compliance, Resources and Client Services, and Wastewater Operations. Our mission is… more
- Bristol Myers Squibb (Princeton, NJ)
- …clinical trials through the review and approval of essential clinical trial and regulatory documents. + Support local regulatory in preparing and performing ... Trial Master File (eTMF) contains the relevant Clinical Trial Package (CTP) regulatory documents for site activation and ongoing study management.t + When… more
- UPMC (Pittsburgh, PA)
- …billing rules as set forth by CMS and other relevant Federal and State regulatory agencies. + Maintain current knowledge and understanding of regulatory trends ... is essential. **Licensure, Certifications, and Clearances:** + Certified Coding Specialist (CCS) + Certified Inpatient Coder (CIC) + Certified Evaluation… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …Product Development (DPD)** Our Drug Product Development team is committed to CMC design, development, and commercialization of innovative drug products to improve ... internal engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and… more