• Manager , CMC Regulatory

    Teva Pharmaceuticals (West Chester, PA)
    Manager , CMC Regulatory Affairs - Remote OR West Chester, PA Date: May 15, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: ... maintaining and updating CMC sections of submissions for assigned products. As Manager CMC Regulatory Affairs you will also be responsible for… more
    Teva Pharmaceuticals (05/16/24)
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  • Director, Regulatory Affairs

    Takeda Pharmaceuticals (Boston, MA)
    …order to bring life-changing therapies to patients worldwide. Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program ... regulations and guidelines by applying interpersonal skills and expert Regulatory Affairs Vaccines (RAV) CMC ...to support their development + May serve as direct/matrix manager of RAV CMC staff, depending on… more
    Takeda Pharmaceuticals (04/18/24)
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  • Manager , Global Regulatory

    Takeda Pharmaceuticals (Lexington, MA)
    …Description** Takeda Development Center Americas, Inc. is seeking a Manager , Global Regulatory Affairs CMC Submissions Management in Lexington, MA with ... changing requirements and priorities; develop/maintain strong working relationships with the regulatory CMC team and cross-functional teams, participate on… more
    Takeda Pharmaceuticals (05/17/24)
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  • Manager , Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …Description** Takeda Development Center Americas, Inc. is seeking a Manager , Global Regulatory Affairs CMC in Cambridge, MA with the following ... requirements: Master's degree in Regulatory Affairs or related field plus 2... representative to provide the assessments. Up to 20% remote work allowed. Full time. $133,200.00 to $223,200.00 /year.… more
    Takeda Pharmaceuticals (05/17/24)
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  • Manager , Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …my knowledge. **Job Description** Takeda Development Center Americas, Inc. is seeking a Manager , Global Regulatory Affairs , Marketed Products in Cambridge, ... the regulatory pathway and history (including competitive regulatory analysis) by researching pre-clinical, clinical, CMC ...Up to 30% domestic travel required. Up to 70% remote work allowed. Full time. $165,500 - $186,000/year Apply… more
    Takeda Pharmaceuticals (06/02/24)
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