• Donor Specialist

    KBR (San Antonio, TX)
    …Donor Specialist Belong. Connect. Grow. With KBR KBR is seeking a Donor Specialist to support our SPARC Program for KBR's Science and Space division. The ... appropriate methods. The goal of this program is to support research that is ongoing at the Uniformed Services...brain injury and chronic traumatic encephalopathy. This is an onsite position, rotating between various partner locations each day.… more
    KBR (12/12/25)
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  • Senior Therapeutic Specialist

    Gilead Sciences, Inc. (Eugene, OR)
    …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... of patients with life-threatening illnesses worldwide. As a **Senior** **Therapeutic Specialist ** within Gilead's - **Eugene, OR** , you will represent Gilead's… more
    Gilead Sciences, Inc. (12/09/25)
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  • Sr Therapeutic Specialist , HIV Treatment…

    Gilead Sciences, Inc. (Houston, TX)
    …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... of patients with life-threatening illnesses worldwide. As a **Sr** **Therapeutic Specialist - HIV** **Treatment** you are responsible for representing Gilead's… more
    Gilead Sciences, Inc. (11/05/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Santa Rosa, CA)
    …in Mounds View, MN or Santa Rosa, CA. The **Senior** **Regulatory Affairs Specialist ** will support our innovative Transcatheter Tricuspid Valve Therapy to treat ... We're working a minimum of 4 days a week onsite as part of our commitment to fostering a...their approval with the agencies. The Sr Regulatory Affairs Specialist is responsible for assessment of device changes for… more
    Medtronic (12/12/25)
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  • Sr. Specialist Regulatory Affairs, MD

    West Pharmaceutical Services (Exton, PA)
    Sr. Specialist Regulatory Affairs, MD Requisition ID: 71773 Date:...a hybrid position requiring the team member to be onsite a minimum of 3 days per week. No ... our sustainability efforts. **Job Summary** The Regulatory Affairs Sr. Specialist is responsible for influencing department regulatory processes and procedures,… more
    West Pharmaceutical Services (11/14/25)
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  • Sr Quality Compliance Specialist

    Abbott (Alameda, CA)
    …with applicable regulatory requirements, including ISO 13485 and MDSAP. The Compliance Specialist will lead and support internal and external audits readiness ... people in more than 160 countries. **Sr Quality Compliance Specialist ** **Working at Abbott** At Abbott, you can do...CA and the individual will be expected to be onsite Monday-Friday. **What You'll Work On** + Maintain and… more
    Abbott (12/03/25)
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  • Business Development Specialist

    Catalent Pharma Solutions (San Diego, CA)
    …Vitamins, and Cosmetics in patient friendly dosage forms. The Business Development Specialist is expected to support the Region's growth by collaborating ... **Business Development Specialist ** **Position Summary** Catalent Pharma and Consumer Health...opportunities that align with Catalent's strategic goals, participate in onsite (in factory) and customer face-to-face meetings with the… more
    Catalent Pharma Solutions (12/11/25)
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  • Sr. Specialist , Regulatory Affairs,…

    West Pharmaceutical Services (Exton, PA)
    …to internal and external customer and/or agency regulatory requests. With minimal support , the Sr. Specialist ensures timely and high-quality execution of ... Sr. Specialist , Regulatory Affairs, Product Stewardship Requisition ID: 69466...Affairs Description: **_This role is a hybrid (3 days onsite ) role however candidates applying must be located within… more
    West Pharmaceutical Services (10/10/25)
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  • Senior Counsel Specialist , Assistant…

    Genentech (South San Francisco, CA)
    …medical devices. As a member of the R&D Law Group, this **"Senior Counsel Specialist , Assistant General Counsel"** role will primarily support Research and Early ... lead legal counsel for global development programs involving innovative scientific initiatives with external collaborators including pharmaceutical manufacturers, digital… more
    Genentech (10/28/25)
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  • Clinical Supply Optimization Specialist

    Sanofi Group (Morristown, NJ)
    **Job Title:** Clinical Supply Optimization Specialist **Location** : Morristown, NJ **About the Job** Are you ready to shape the future of medicine? The race is on ... so that trial implementation is not disrupted. As a Clinical Supply Optimization Specialist (CSOS) within the CSC-PM team, you will be accountable to identify an… more
    Sanofi Group (12/15/25)
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