• Technical Specialist

    Pfizer (Andover, MA)
    …have the medicines they need, when they need them. **What You Will Achieve** The clinical manufacturing technical specialist is part of a ... clinical , and launch activities. This role is a key communication and technical interface between the GMP manufacturing teams in the plant and our… more
    Pfizer (10/31/24)
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  • Sr. GTM Specialist , Therapeutic…

    Amazon (Boston, MA)
    …experience (10+ years) in a Biopharma or Healthcare company - - Commercial, Clinical Trials, Manufacturing experience highly valued - - Experience in BD, ... for healthcare + life sciences (HCLS) customers? Within SMGS, the Worldwide Specialist Organization (WWSO) works backwards from our customers' most complex and… more
    Amazon (10/17/24)
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  • Sr Manufacturing Specialist

    Astellas Pharma (Westborough, MA)
    **Sr Manufacturing Specialist , Production Planning** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every ... AIRM is headquartered in Massachusetts. Astellas is announcing a **Sr Manufacturing Specialist , Production Planning** opportunity at their **Astellas Institute… more
    Astellas Pharma (09/19/24)
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  • Senior Specialist , Clinical

    Merck (Boston, MA)
    …Skills: strong knowledge of the principles of project management and clinical customer relationship management. + Technical Proficiency: familiarity with ... + Proven record in project / portfolio management. + Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP) is highly desirable.… more
    Merck (10/31/24)
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  • Senior Validation Specialist , Quality…

    Astellas Pharma (Westborough, MA)
    …of commissioning, qualification and validation support to M-TC's cGMP Cell Therapy Manufacturing facility as the products move through clinical trials and ... following:** + Individual Contributor responsible to execute QA Validation Strategy for clinical and pre-commercial cell and gene therapy manufacturing facility.… more
    Astellas Pharma (09/05/24)
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  • Compliance Specialist

    Astellas Pharma (Westborough, MA)
    Specialist will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. The ... **Compliance Specialist ** Do you want to be part of...years of industry experience in biotechnological and/or pharmaceutical quality, manufacturing , or other industry requiring high technical more
    Astellas Pharma (10/06/24)
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  • Facility Engineering Compliance Specialist

    Astellas Pharma (Westborough, MA)
    **Facility Engineering Compliance Specialist ** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are ... range of disease indications, ranging from macular degeneration (currently in clinical trials) and other ocular indications to vascular and autoimmune disease.… more
    Astellas Pharma (09/13/24)
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  • Quality Assurance, Compliance Specialist

    Astellas Pharma (Westborough, MA)
    …Assurance team will perform critical QA compliance tasks in support of GMP manufacturing programs as AIRM moves through clinical trials and commercialization. ... **QA Compliance Specialist ** Do you want to be part of...of disease indications, ranging from macular degeneration (currently in clinical trials) and other ocular indications to vascular and… more
    Astellas Pharma (09/18/24)
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  • Senior Document Specialist

    Astellas Pharma (Westborough, MA)
    …for Regenerative Medicine (AIRM)** site in **Westborough, MA.** **Purpose:** The Specialist , Document Control has responsibilities the technical and ... **Senior Document Specialist ** Do you want to be part of...of disease indications, ranging from macular degeneration (currently in clinical trials) and other ocular indications to vascular and… more
    Astellas Pharma (08/22/24)
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  • QA Specialist I - Operations

    PCI Pharma Services (Bedford, NH)
    …network to pioneer and shape the future of PCI. Job Summary: The QA Specialist will work with other departments to ensure the quality of products and compliance ... programs by providing QA expertise and guidance to the manufacture of both clinical and commercial products. **Job Duties** + Perform review of batch documentation… more
    PCI Pharma Services (10/17/24)
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  • Principal Regulatory Affairs Specialist

    Philips (Cambridge, MA)
    The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies and post market changes for complex, ... Provide guidance on global compliance such as CE Marking and product registrations, clinical evaluations in accordance with EU MDR, ISO 13485, and ISO 14155, China… more
    Philips (10/17/24)
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  • Metrology Specialist

    Bristol Myers Squibb (Devens, MA)
    …personal lives. Read more: careers.bms.com/working-with-us . **Position:** **Metrology Specialist ** **Location: Devens, MA** **Rotational Shift 12-hours for 6am ... in emergency on-call rotation as required to support operations. 5. Provides technical support as Metrology SME for engineering projects towards improvement of… more
    Bristol Myers Squibb (10/23/24)
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  • Post Market Surveillance Senior Specialist

    ZOLL Medical Corporation (Chelmsford, MA)
    …Surveillance program designed to meet FDA's Quality System Regulation (QSR)/ Good Manufacturing Practices (GMP), MDD, EU MDR, MDSAP, and the globally harmonized ... will work with surrounding departments such as Quality Assurance, Compliance, Technical Support, Service, and Regulatory Affairs. Involved in several aspects of… more
    ZOLL Medical Corporation (10/09/24)
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  • Supervisor, Laboratory CLIA Operations

    Bio-Techne (Waltham, MA)
    …and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing , and testing services. Our family of brands creates a unique ... and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers… more
    Bio-Techne (10/15/24)
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  • Licensed Practical Nurse LPN

    BioLife Plasma Services (Methuen, MA)
    …will be familiar with regulations of the plasma collection industry or a manufacturing environment. The Medical Support Specialist follows guidance provided by ... unacceptable findings to donors, or guidance concerning medical or technical issues, including donor safety and eligibility. + You...the FDA approved training requirements for BioLife Medical Support Specialist + Two years in a clinical more
    BioLife Plasma Services (09/01/24)
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  • Field Service Engineer (Field Base Woburn, MA)

    BD (Becton, Dickinson and Company) (Woburn, MA)
    …site. + Timely escalate all customer and/or instrument related issues to District Technical Specialist and Service Manager for additional support. + Promote and ... of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products...support, holiday and weekend on-site support, marketing, exhibitions, and clinical trials support. Within the role of an FSE,… more
    BD (Becton, Dickinson and Company) (10/26/24)
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  • Sr Software Systems Engineer - Surgical Robotics

    Medtronic (Boston, MA)
    …product R&D and clinical /regulatory process + Fluency in English ** TECHNICAL SPECIALIST CAREER STREAM:** An individual contributor with responsibility in ... support and assistance during usability studies, preclinical labs and/or manufacturing processes + Contribute to development and maintenance of...our technical functions to advance existing technology or introduce new… more
    Medtronic (10/23/24)
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  • Field Application Scientist - Boston Area

    Bio-Techne (Waltham, MA)
    …and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing , and testing services. Our family of brands creates a unique ... and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers… more
    Bio-Techne (10/25/24)
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