• Merck & Co. (Rahway, NJ)
    …regulatory updates.Audit vendors/partners of SaMD/IVD/Companion DiagnosticsReports to - Director Regulatory Compliance, Device Quality and RegulatoryLocation - ... combination products.Prefer at least 3 years demonstrated leadership experience with project teamsCurrent Employees apply HERE Current Contingent Workers apply HERE… more
    HireLifeScience (06/24/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the ... as point of contact to cross-functional teams on US/EU RA CMC project issues.Execution of Strategy and Submissions: Develops strategy with supervision. Prepares… more
    HireLifeScience (05/15/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC , and Clinical Development to collate the necessary information to ... participate/contribute to discussions in applicable working teams, technical teams, project teams, etc. Qualifications: Successful candidates will be able to… more
    HireLifeScience (05/18/25)
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  • Associate Director , CMC

    WuXi AppTec (Cranbury, NJ)
    **Overview** STA Pharmaceutical, a WuXi AppTec Company, has an exciting opportunity for an ** Associate Director , CMC Project Management.** This position ... lead the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development… more
    WuXi AppTec (06/04/25)
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  • Associate Director , CMC

    WuXi AppTec (Cranbury, NJ)
    **Overview** The AD Project Manager will be responsible for managing projects within STA, WuXi's API, and Drug Product development and manufacturing division. Leads ... the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team.… more
    WuXi AppTec (06/17/25)
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  • Associate Principal Scientist/…

    Merck (Rahway, NJ)
    …+ Audit vendors/partners of SaMD/IVD/Companion Diagnostics **Reports to** - Director Regulatory Compliance, Device Quality and Regulatory **Location** - Remote, ... Prefer at least 3 years demonstrated leadership experience with project teams Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld) Current Contingent… more
    Merck (06/24/25)
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  • Sr. Principal/ Associate Director

    Bristol Myers Squibb (Summit, NJ)
    …but not limited to, continued process verification. The role collaborates across all CMC functional areas to ensure project advancement, rapid and best in ... for process risks + Able to manage time and elevate relevant issues to project lead and line management. + Detail oriented with excellent verbal and written… more
    Bristol Myers Squibb (06/24/25)
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