Takeda Development Center Americas, Inc Cambridge, Massachusetts, 02142 Takeda Development Center Americas Inc. seeking an Associate Director, CMC Program Lead, Cell Therapies in Cambridge, MA with the following duties: Lead a Chemistry, Manufacturing and Control (CMC) matrix teams to deliver Cell Therapy pipeline projects. Up to 60 percent remote work allowed. Full time. $221,900.00 - $255,600.00 /year. Apply on-line at https://jobs.takeda.com and search for Req #R01 |
Center for Biostatistics in AIDS Research (CBAR) BOSTON, Massachusetts, 02115 Position Description The The Center for Biostatistics in AIDS Research (CBAR) Finance Team is seeking an Associate Director of Finance and Grants Administration. This position, which reports to the Executive Director for Finance, Administration and Information Technology (EDFAI), will oversee the Center's funding. This role requires a self-directed individual, who can work collaboratively with Pri |
Joulé Allentown, Pennsylvania, 18109 Title: Associate Director, Quality Engineering Location: Allentown, Pa Schedule: M-F 8am-5 pm (on-site) Type: Direct/Permanent Salary Range: 150,000-160,000 + 15% bonus and full relocation package if needed Start date: Immediate Are you a strategic leader with a passion for driving quality excellence? This Associate Director role offers the chance to make a significant impact by overseeing two ess |
Innova Solutions Foster City, California Innova Solutions has a client that is immediately hiring for Associate Director, Field Leadership Sales Training. Position type: Fulltime - Contract Duration: 18 Months Location: Remote As Associate Director, Field Leadership Sales Training, you will: Job Description: Essential Duties and Job Functions: * Experience in curriculum development, project management, executive presence, facilitation ex |
Takeda Development Center Americas, Inc Cambridge, Massachusetts, 02142 Takeda Development Center Americas, Inc. is seeking a Associate Director, Global Regulatory Affairs in Cambridge, MA to Oversee as well as execute all regulatory activities of multiple projects including one highly complex project in development and/or support regulatory activities for assigned marketed product(s) of responsibility. Up to 20% domestic and international travel required. Full time. |