- Takeda Pharmaceuticals (Boston, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... under the TAUs. The role will also drive best practices and process improvements cross-functionally to enhance clinical trial efficiency. Seen as a clinical… more
- Gilead Sciences, Inc. (Foster City, CA)
- …all lines of business and payers. + Serve as HCV/HBV subject matter expert cross-functionally with the Business Unit, Medical, Analytics, and others. + Provide ... Other Roles and Responsibilities: + Develop understanding of Gilead's PRC process , including management of materials in Veeva, to shepherd materials through… more
- Unither Pharmaceuticals (Rochester, NY)
- …A, B & C shifts available Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify ... Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 280 employees.… more
- IQVIA (Durham, NC)
- …to drive quality statistical planning, analysis, and reporting in support of pharmaceutical development and regulatory submissions. Serve as a resource for the ... - Lead studies at an operational level. - Provide expert review and initiate methodology development work with regards...lead in implementing risk mitigation actions. **Lock and Unblinding Process :** - Lead the database lock and unblinding … more
- Lilly (IN)
- …precedence. **1.** **Case Management Leadership** + Serve as a leading technical expert in Individual Case Safety Reporting (ICSR) and case management, providing ... advice to support sound business decisions and regulatory compliance. + Deliver expert insight on best practices, emerging trends and partner with internal… more
- Mallinckrodt Pharmaceuticals (St. Louis, MO)
- …site and corporate objectives. Specifically, this position will oversee 24/7 in- process laboratory testing, data release of raw materials, intermediates, stability, ... improvement and enhancement + Serve as the Subject Matter Expert during compliance audits + Study and improve various...and improve various Quality processes through increased efficiency or process flow using Lean Manufacturing and/ or Six Sigma… more
- Teva Pharmaceuticals (West Chester, PA)
- …strict confidentiality. This position will serve as a subject matter expert on investigations, applying and maintaining progressive knowledge of investigative ... with utmost discretion, objectivity and sensitivity. + Serve as subject matter expert on forensic accounting investigative techniques. Maintain expert knowledge… more
- GRAIL (Durham, NC)
- …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... . Grail's Clinical Compliance department is seeking a compliance expert to support compliant conduct of Grail's clinical studies and to support Grail's partnerships… more
- J&J Family of Companies (Raritan, NJ)
- …https://www.jnj.com **Job Function:** Supply Chain Engineering **Job Sub** **Function:** Process Engineering **Job Category:** People Leader **All Job Posting ... Spring House, PA. **Purpose:** The Technical Fellow serves as a subject matter expert (SME) in CAR-T manufacturing and Quality Control analysis, playing a pivotal… more
- Charles River Laboratories (Reno, NV)
- …business with an agile and customer-centric mindset that drives process improvement, efficiencies, effective and timely customer response, and customer-centered ... ten years experience in scientific and management in the life sciences, pharmaceutical , or contract research fields. + Knowledge of business and operations… more
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