- Lilly (Indianapolis, IN)
- …support for Clinical Trial Applications, Market Registrations And Post-Approval Submissions. The Research Scientist in Global Regulatory Affairs - CMC will ... world. We are seeking an Advisor/Senior Advisor for Global Regulatory Affairs CMC to be a part...CMC strategies and develop submissions for marketing authorizations. The Regulatory Scientist is expected to develop and… more
- Abbott (St. Paul, MN)
- …holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs , and external stake ... 114,000 colleagues serve people in more than 160 countries. **Senior Principal Clinical Scientist ** **Working at Abbott** At Abbott, you can do work that matters,… more
- J&J Family of Companies (Skillman, NJ)
- …Collaboration:** * Work closely with Supply Chain, R&D, Quality Assurance, Regulatory Affairs , and other departments. * Foster effective communication ... MS&T Process Scientist 2 - 2407025323W **Description** Kenvue is currently...reports to:** Manager, Process Science **Location:** Skillman, NJ _Kenvues corporate headquarters is currently located in_ _Skillman,_ _NJ_ _,… more
- J&J Family of Companies (Skillman, NJ)
- …Collaboration:** * Work closely with Supply Chain, R&D, Quality Assurance, Regulatory Affairs , and other departments. * Foster effective communication ... Senior Scientist Technical Operations - 2407024955W **Description** Kenvue is...to:** Senior Manager, Process Science **Location:** Skillman NJ _Kenvues corporate headquarters is currently located in_ _Skillman_ _NJ_ _,… more
- Herbalife (Winston Salem, NC)
- …routinely with Herbalife global cross functional teams including Quality, Procurement, Regulatory Affairs , Project Management and Supply Chain as well ... Sr. Research Scientist , Process & Manufacturing Category: Scientific & Medical...launches, smooth commercial production, and compliance with quality and regulatory standards as well as on target profit margin.… more
- Herbalife (Torrance, CA)
- …with Herbalife global cross functional teams including Innovation, Quality, Product Sourcing, Regulatory Affairs , Project Management and Supply Chain as well as ... Research Scientist , Process & Manufacturing Excellence Category: Research &...and formula specifications to meet quality, uniformity, safety and regulatory requirements; evaluating new process, equipment and technology that… more
- Abbott (Abbott Park, IL)
- …stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs as well as ... and management solutions for treating structural heart disease. As the Principal Clinical Scientist , you'll have the chance to work closely with the clinical study… more
- AbbVie (North Chicago, IL)
- …disciplines to further program goals via collaborations with drug product development, regulatory affairs , and commercial operations. + The candidate will ... development of AbbVie's clinical candidates. We are seeking a Principal Research Scientist II to conduct process research and development of antibody-drug conjugates… more
- AbbVie (North Chicago, IL)
- …with many groups external to PDS&T, for example: Manufacturing Operations, Regulatory Affairs , Quality Assurance, etc. Responsibilities: + The candidate ... and throughout the product lifecycle. PDS&T is seeking a Principal Research Scientist (Chemistry) who is highly motivated, with a proven track record of… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... while developing and expanding your career. The Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... colleagues while developing and expanding your career. The Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, ... The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …including working with contract manufacturing organizations CMO.** This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- Valent BioSciences (Libertyville, IL)
- …close collaboration with internal functional groups, including Global Research, Regulatory Affairs , Marketing/Business Management, Manufacturing and Project ... around new products and uses where possible. Provides technical support to Regulatory Affairs for domestic and international product registrations, including the… more
- AbbVie (North Chicago, IL)
- …across Small Molecule and Biologics Analytical R&D functions (SMARD/BARD), CMC Regulatory Affairs (RA), Quality Assurance (QA), CMC Coordination, Product ... and risk to make decisions having mid-term impact. Ensures alignment with corporate / regulatory policies/standards. + Steps up and takes leadership to implement… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …+ Interact with clinical investigators and thought leaders + Work with internal regulatory affairs team and other ethical guidelines relevant to the ... Work in a team environment comprising clinical operations, biomarker specialists, CROs, and regulatory affairs + Provide clinical expertise and input for … more
- Gilead Sciences, Inc. (Foster City, CA)
- …Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs , Quality Control and Manufacturing Operations by providing ... development. The role is satisfied by an experienced leader and scientist responsible for shaping the development strategy for analytical methods, implementing… more
- Merck (San Diego, CA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Clinical Director (Principal Scientist ) has primary responsibility for planning and directing clinical research activities involving… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... and expanding your career. The Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research… more
- Vanderbilt University (Nashville, TN)
- …with CTTC licensing officers and staff. Reporting directly to the Corporate Contracts Manager, the Contracts Officer negotiates various technology transfer ... agreements on intellectual property and to negotiate practical resolutions that balance scientist and industry needs with the mission of CTTC. + Aids in… more