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Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
... permanent Quality Operations Senior Compliance Specialist to provide quality and compliance ... that appropriate BMS GMP and regulatory standards are adhered to for ... functional groups such as Global..
Assist Regulatory manager for implementing and delivering ... manager for implementing and delivering regulatory submission and approval, and maintenance ... area within agreed timeline. Ensure regulatory compliance with government policy..
... currently looking to fill a CMC Regulatory Sciences Specialist position, this position is responsible ... providing Chemistry, Manufacturing, and Controls (CMC) support across Regeneron’s sites. Routine ... post approval..
Major Responsibilities: Assist Regulatory manager for implementing and delivering ... manager for implementing and delivering regulatory submission and approval, and maintenance ... area within agreed timeline. Ensure regulatory compliance with..
Medical Editor II Come discover what our 25,000 employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to work ..
... be proud of. Join us.Director, CMC StatisticsLiveWhat you will doLets do ... across different therapeutic areas.The Director, CMC Statistics, will manage, act as ... quality oversight of the Global..
... We are looking for the Regulatory Affairs Specialist who will be working with ... manage new product submissions for regulatory approval to the local Health ... Authority (HA). Liaise..
Position: Principal Scientist, CMC- Analytical DevelopmentrnReports to: Director, Analytical ... as other functions including Manufacturing, CMC team, Project Development and Regulatory, to ensure the timely development, ... later NDAs, BLAs,..
... Bristol Myers Squibb QA Senior Specialist, Actives and Intermediates in Dublin ... recruit a permanent QA Senior Specialist , Actives & Intermediates based ... Global market. The QA Senior..
Director of Regulatory Affairs (Strategy) Salary: Highly Competitive ... is seeking a Director of Regulatory Affairs (Strategy) for a leading ... overall clinical and nonclinical global regulatory strategy across the..
... control to ensure we meet regulatory standards, and procure the needed ... meaningful impact on patientsu2019 lives.QCAT Specialist - Shanbally, Ringaskiddy, CorkSpecialist u2013 ... Managementu00A0The Global Stability Program Management..
Position: Principal Engineer, Biologics Development rnReports to: Associate Director, Biologics DevelopmentrnLocation: Brisbane, CA (Remote-US)rnrnSummaryrnrnAimmune Therapeutics is looking for a talented senior/principal engineer to support the early-stage biologics programs (i.e. monoclonal antibodies, ..
... offer the highest quality and regulatory capabilities, and flexible and adaptive ... archival and destruction. The Quality Specialist is a key quality function ... relationships and collaborate closely with..
Position: Specialist/Sr. Specialist, Clinical Manufacturing & Supply ChainrnReports ... Clinical Manufacturing & Supply Chain Specialist will work as an integral ... stakeholders, such as Clinical Operations, Regulatory Affairs, Quality Assurance,..
... a permanent Quality Operations Senior Specialist Drug Product to p rovide ... functional groups such as Global Regulatory/CMC and the local country based ... and the local country based..
... located in Waltham, Massachusetts.rnrnSummaryrnrnThe Operations Specialist, Nonclinical Development is responsible for ... to support nonclinical reports and regulatory submissions.rnrnThe Operations Specialist, Nonclinical Development will work closely ... will work..
Summary Provides regulatory guidance that shapes the direction ... direction of BMS teams (e.g., Regulatory Team, Multi functional Development team, ... Recognized as a Leader in Regulatory Science and credible..
... for clarification or revision Assures regulatory guidelines are followed for electronic ... Demonstrates a working knowledge of regulatory practices and requirements and supports ... and requirements and supports other..
... Omeros!n nCome join our Omeros CMC Team!n nAbout Omeros CorporationnOmeros is ... subject matter expertnAssists in trouble-shooting CMC-related problems from CROs / CMOsnAssists ... and/or GMP environmentsnContribute to drafting..
The Role:Moderna is seeking a Quality Assurance Manager reporting to the Sr. Manager Quality Assurance. The individual in this role will be responsible for providing Quality leadership & support and lead ..
... get Ahead Together. Job Title Specialist, CMC Vx Mature Products In this ... the timely preparation of technical (CMC) regulatory documents for lifecycle activities and ... in accordance with..