• Oncology Territory Manager, Solid Tumors…

    Takeda Pharmaceuticals (TN)
    …I submit in my employment application is true to the best of my knowledge . **Job Description** **About the role:** As a member of Takeda Oncology your work ... Oncology Sales team, you will report to the Regional Director and work with key stakeholders. **How you will...on market conditions to Home Office colleagues for the development of targeted marketing strategies and materials + Focus… more
    Takeda Pharmaceuticals (09/17/25)
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  • Computer Systems Validation Specialist

    Unither Pharmaceuticals (Rochester, NY)
    Computer Systems Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve ... Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 280 employees.… more
    Unither Pharmaceuticals (08/27/25)
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  • Quality Supervisor

    BioLife Plasma Services (Social Circle, GA)
    …I submit in my employment application is true to the best of my knowledge . **Job Description** **About BioLife Plasma** Takeda offers a purpose you can believe in, ... you. At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best-in-class patient support programs. Takeda… more
    BioLife Plasma Services (08/01/25)
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  • Senior cGMP Specialist- Quality Control Analytical…

    Houston Methodist (Houston, TX)
    …our patients and customers. Additional Skillset is preferred: + Demonstrated knowledge and experience in analytical procedure development , validation, instrument ... As a senior member of the department, this position will actively contribute to the development of policies and procedures for the delivery of novel products to… more
    Houston Methodist (08/13/25)
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  • Senior Manager Regional Regulatory Lead - US…

    CSL Behring (King Of Prussia, PA)
    …**Candidates have developing knowledge and understanding of pharmaceutical /biological product development and regulatory requirements for product ... onsite three days a week. You will report to the Executive Director Head Regulatory. **Position Description** **Summary** **Regulatory leaders who leverage regional… more
    CSL Behring (09/16/25)
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  • Receiving Clerk

    Charles River Laboratories (Rockville, MD)
    …75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, ... required for various client projects under the guidance of the Associate Director Materials Management. They will also interact with Charles River Laboratories raw… more
    Charles River Laboratories (09/05/25)
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  • Project Manager

    Teledyne (Lincoln, NE)
    …air and water quality environmental monitoring, electronics design and development , oceanographic research, energy, medical imaging and pharmaceutical ... air and water quality environmental monitoring, electronics design and development , oceanographic research, deepwater oil and gas exploration and production,… more
    Teledyne (07/29/25)
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  • Research Scientist Postdoctoral Tri Researcher

    AdventHealth (Orlando, FL)
    …as evidenced by published (peer reviewed) research and/or prior work experience. o Knowledge of the development and operation of clinical and basic science ... - Paid Days Off from Day One - Career Development - Whole Person Wellbeing Resources - Mental Health...protocols . **Preferred qualifications:** o Proven history of NIH, Pharmaceutical and/or equivalent research o Knowledge or… more
    AdventHealth (08/07/25)
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  • Sr. Manager - QA Incoming Batch Disposition

    Lilly (Durham, NC)
    …site inspection readiness and execution. The Manager reports to the Associate Director -Materials QA. **Key Objectives and Deliverables:** + Support the site to ... promoting teamwork and employee participation in the work group + Support the development of the overall site operational readiness plan including development of… more
    Lilly (09/18/25)
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  • Senior Clinical Scientist - Ophthalmology

    Merck (North Wales, PA)
    …and presentation skills **Education/Experience** Bachelor's Degree +5 years of pharmaceutical , clinical drug development , project management, and/or medical ... field experience OR Master's Degree +3 year of pharmaceutical , clinical drug development , project management, and/or medical field experience OR PhD/PharmD… more
    Merck (09/05/25)
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