- Gilead Sciences, Inc. (Foster City, CA)
- …countries worldwide, with headquarters in Foster City, California. **TITLE:** **Senior Director , Analytical Lifecycle Management - Biologics Quality Control ... biologics drug substances and drug products. The Senior Director collaborates with cross-functional teams, fosters a culture of continuous improvement,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in more than 35 countries worldwide, with headquarters in Foster City, California. ** Director , CMC Regulatory Affairs - Biologics ** **KEY RESPONSIBILITIES** The ... Director , CMC Regulatory Affairs for Biologics is responsible for defining regulatory strategy for one...for a single or multiple products. + Lead the execution and influence the development of global CMC regulatory… more
- Gilead Sciences, Inc. (Foster City, CA)
- …more than 35 countries worldwide, with headquarters in Foster City, California. ** Director , Strategic Sourcing and Supplier Management, Biologics DP** **KEY ... RESPONSIBILITIES** The Director , Strategic Sourcing & Supplier Management, Biologics DP owns the strategic business relationship with multiple contract… more
- Gilead Sciences, Inc. (Foster City, CA)
- …help create possible, together. **Job Description** **Key Responsibilities** Associate Director , Global External Manufacturing Biologics ensures uninterrupted ... supply of Gilead's clinical and commercial products through execution of manufacturing campaigns within our global external contract manufacturing network, while… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **Key Responsibilities:** Senior Director , Global External Manufacturing, Biologics will lead an ... supply of Gilead's clinical and commercial biologic products through execution of manufacturing campaigns within our global external contract manufacturing… more
- Sumitomo Pharma (Morrisville, NC)
- … execution , and final approval. + Create and maintain cell biologics - medical device combination product design history files from early-stage development ... **Sr. Director , Cell Quality** Sumitomo Pharma America (SMPA) is...and Responsibilities** + Provide Quality leadership on planning and execution for the build out, commissioning, and on-going support… more
- Boehringer Ingelheim (Ridgefield, CT)
- …programs reflect Boehringer Ingelheim's high regard for our employees. The Director , Global Regulatory Strategy Lead will provide strategic regulatory guidance and ... represent Global Regulatory Affairs (GRA) on the Evidence Team. The Director , Global Regulatory Strategy Lead will craft comprehensive, well-thought through… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …real-world evidence, and creating hope for all facing illness. As a senior memberof Medical Science, theSenior Director , Medical Science will lead the early- ... areas involving complex indications including rare disease/orphan conditions. The Senior Director , Medical Science will be responsible for clinical development… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary** The Senior Director , Global Oncology Medical Affairs is responsible for developing the ... the assigned compound or therapeutic area and leads development, execution of the Global Medical Affairs plan...one time required - Knowledge of ADC or other biologics , or small molecules preferred - Demonstrated experience working… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary** The Senior Director , Global Oncology Medical Affairs is responsible for developing the ... the assigned compound or therapeutic area and leads development, execution of the Global Medical Affairs plan...at one time required -Knowledge of ADC or other biologics , or small molecules preferred -Demonstrated experience working with… more
- Bristol Myers Squibb (Manati, PR)
- …role will provide strategic HR Business Partner leadership to support the local Biologics Operations Leadership Team, in their execution of the Global Product ... their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The HR Director for the Manati, Puerto Rico site will establish the HR… more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. Join Takeda as a Director , Regulatory Affairs Vaccines CMC where you will provide program leadership and ... with strategic partners globally. **How you will contribute:** + Lead planning, execution , and management of regulatory submissions for assigned vaccines in various… more
- Boehringer Ingelheim (Ridgefield, CT)
- …shape early target label profiles and oversee the planning, preparation, and execution of regulatory submissions. Your role will also involve supporting submission ... sciences or chemistry with 7 years experience in regulated pharmaceutical industry ( biologics or small-molecule) + Preferred: Master's Degree or Doctoral Degree (eg… more
- AbbVie (Worcester, MA)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Job Description AbbVie Bioresearch Center (ABC) is hiring an Associate Director Automation & Manufacturing Systems position to lead the Operational Technology… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC has discovered and produced several ... treatments for difficult-to-treat diseases and commercializing products with significant unmet medical needs in North American markets. In the United States, MTPA… more
- Gilead Sciences, Inc. (Foster City, CA)
- …worldwide, with headquarters in Foster City, California. **Senior Director , Strategic Sourcing and Supplier Management, Contracting** **KEY RESPONSIBILITIES** ... The Sr. Director , Contracting is accountable for the processes, systems, and...processes, systems, and strategies utilized in the negotiation and execution of contracts with contract development and manufacturing organizations… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Regulatory Affairs - West Chester, PA Date: Mar 26, 2024 Location: West Chester, United States, 1938 Company: Teva Pharmaceuticals Job Id: 54230 ... with. **How you'll spend your day** As the Associate Director , Regulatory Affairs you will be responsible for acting...(CDT), and CMC Team to ensure successful planning and execution of the global regulatory strategy for assigned projects.… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, atopic dermatitis, ... candidates in development in other areas of high unmet medical need. **A Typical Day Might Look Like This:**...of the brand and will report to the Senior Director , Respiratory Marketing Market Development Lead. The candidate will… more
- System One (Deland, FL)
- Position: CONTRACTOR -- Director , US Regulatory Affairs & Global Development Projects (GDP) Location: Remote (East or Central Time Zone) / Prefers local Contract: ... 12mns Pay Rate: 80/hr - 95/hr Purpose and Scope of Position The Director , US Regulatory Affairs & Global Development Projects (GDP) is responsible for providing… more
- Publicis Groupe (New York, NY)
- …5 of the top 8 pharma companies on our roster. **Job Description** The VP, Account Director is responsible for the day to day running of one of the largest accounts, ... and profitability while proactively managing and developing team members. The VP, Account Director is expected to be a strategic client contact and advisor, with… more