• Post-Doctoral Fellow - Medical Affairs…

    Boehringer Ingelheim (Ridgefield, CT)
    …Additional Attachments. **Desired Skills, Experience and Abilities** + Prior pharmaceutical industry experience (eg internship or Advanced Pharmacy Practice ... educational materials, train internal medical team members, and disseminate data from scientific manuscripts, congresses, etc. + Collaborate cross-functionally with… more
    Boehringer Ingelheim (08/30/25)
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  • Finance Manager

    Teledyne (Mountain View, CA)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... TMS as well as rolling forecast model, annual and 3-year strategic plan + Review revenue check list that determines the revenue recognition checklist and review more
    Teledyne (07/29/25)
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  • In-Process Quality Engineer

    Mallinckrodt Pharmaceuticals (St. Louis, MO)
    …Supply Chain, and other Quality groups. Job Description ESSENTIAL FUNCTIONS: + Review and approve Exception and OOS investigations, CAPAs, Change Controls, and ... Customer Complaints in TrackWise system + Generate data for Annual Product Reviews + Organize and document...for Annual Product Reviews + Organize and document Material Review Boards for product disposition + Review more
    Mallinckrodt Pharmaceuticals (07/03/25)
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  • Associate Director, Vendor Audits

    Bristol Myers Squibb (Princeton, NJ)
    …service provider concerning quality and compliance issues, conduct periodic strategy review meetings, manage escalations, review audit dashboards, and ... required. + A minimum of eight (8) years' experience in the Biopharm/ Pharmaceutical industry with in-depth knowledge and experience in global auditing procedures and… more
    Bristol Myers Squibb (09/12/25)
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  • Director, Global Biopharmaceutical Stability…

    Bristol Myers Squibb (Princeton, NJ)
    …this position will have team oversight for the implementation and improvement of Data Integrity requirements and Quality Risk Management tools. This position is also ... Biopharmaceutical Stability trend program including initial site implementation, periodic review , and the definition and implementation of electronic solutions for… more
    Bristol Myers Squibb (09/11/25)
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  • Associate, Clinical Trial

    Sumitomo Pharma (Cheyenne, WY)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... completion of all study deliverables, ensuring the highest level of data quality; proactively identifies, communicates, and resolves clinical study operational… more
    Sumitomo Pharma (09/10/25)
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  • Senior Scientist, Quality Control

    Amneal Pharmaceuticals (Piscataway, NJ)
    …and report results. Actively participate in investigation of laboratory results. Review laboratory analysis data for completeness, specification compliance, and ... for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following… more
    Amneal Pharmaceuticals (09/09/25)
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  • Supply Planner

    Dr. Reddy's Laboratories (Princeton, NJ)
    …minimize excess inventory.* Analyze weekly and monthly demand using order and forecast data to adjust packing plans accordingly.* Review monthly supply gaps and ... packaging at co-packer facilities.* Manage co-packer operations to ensure timely creation, review , and release of finished goods batch documents.* Create batches for… more
    Dr. Reddy's Laboratories (09/04/25)
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  • Associate Director, Research Business Excellence

    Takeda Pharmaceuticals (Boston, MA)
    …Excellence in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... and optimization of teams within Research. The incumbent will drive continuous review and reporting of Research business activities and support operational needs of… more
    Takeda Pharmaceuticals (08/16/25)
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  • CSV Automation Specialist

    VTI Life Sciences (San Diego, CA)
    …and ambitious engineers looking to accelerate their career in the pharmaceutical , biotechnology and medical device industries. We offer an opportunity to ... industry standards, regulatory requirements (such as FDA 21 CFR Part 11 and 820, Data Integrity, ISO 13485 and GAMP 5.), and company policies. The role includes the… more
    VTI Life Sciences (08/13/25)
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