• Head of Business Management Biopharma

    BASF (Florham Park, NJ)
    …release criteria for existing products and new product developments. Provides technical support to production and supports continuous product quality improvement ... by initiating appropriate measures. + Ensuring the regulatory fit of existing and new Biopharma products and supporting the definition of the regulatory more
    BASF (05/02/24)
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  • Product Marketing Manager, Biopharma

    ThermoFisher Scientific (WV)
    …biopharmaceutical, and optionally, omics, markets. You will deliver high value, high quality marketing collateral to support our go-to-market strategies. You ... biopharma including, impactful customer-facing marketing collateral, sales and support trainings for product positioning to internal and external customers and… more
    ThermoFisher Scientific (04/07/24)
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  • Biopharma Exception Report Investigation…

    AbbVie (Worcester, MA)
    …We are seeking a highly motivated candidate to join our team as the Biopharma Investigation Author. The Sr Specialist Quality Systems is responsible for ... providing quality assurance support for some or all of the following manufacturing...in as many of the following areas as possible: Quality , Regulatory , Process Sciences, Manufacturing Operations. +… more
    AbbVie (05/01/24)
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  • Quality Operations Specialist

    Kedrion Biopharma, Inc. (Melville, NY)
    …information and trends. **Other:** + Support audits conducted by clients or regulatory / agencies. + Support regulatory submissions if applicable. + ... Kedrion Biopharma is a biopharmaceutical company specializing in the...quality and production related documentation and procedures in support of internal manufacturing operations. The position advises … more
    Kedrion Biopharma, Inc. (02/24/24)
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  • Scientist Biopharma Manufacturing

    Astellas Pharma (Westborough, MA)
    …AIRM is headquartered in Massachusetts. Astellas is announcing a **Technical Biopharma Manufacturing Scientist I** opportunity at their **Astellas Institute for ... candidate will work closely with Process Development, Manufacturing, Engineering and Quality Assurance teams to ensure successful introduction of new processes (NPI)… more
    Astellas Pharma (04/19/24)
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  • Engineering Manager

    Kedrion Biopharma, Inc. (Melville, NY)
    …repository to capture and apply insights from past project risks and mitigations. ** Regulatory Compliance and Quality Assurance** + Ensure that all capital ... Kedrion Biopharma is a biopharmaceutical company specializing in the...Collaborate with cross-functional teams, including engineering, operations, finance, and regulatory affairs, to conduct in-depth feasibility studies, risk assessments,… more
    Kedrion Biopharma, Inc. (03/01/24)
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  • Administrative Assistant

    Kedrion Biopharma, Inc. (Fort Lee, NJ)
    …and mailing or shipments from the site, ie new employee onboarding or offboarding, support of regulatory or quality documents, scheduling interviews, org ... Kedrion Biopharma is a biopharmaceutical company specializing in the...in this role include: + Executive and VP level support for travel arrangements, expense reports, calendar management, … more
    Kedrion Biopharma, Inc. (03/15/24)
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  • Senior Representative, Regulatory Affairs

    Catalent Pharma Solutions (Bloomington, IN)
    **We're hiring for a Senior Regulatory Affairs Specialist to support compliance and regulatory affairs in Bloomington, Indiana!** Catalent is a global, ... update facility drug master files. + Prepare accurate and quality documentation for client regulatory submissions. +...documentation for client regulatory submissions. + Provide regulatory guidance and support for development and… more
    Catalent Pharma Solutions (04/10/24)
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  • Associate Director, Regulatory Affairs

    Catalent Pharma Solutions (Hillside, NJ)
    …patient, consumer and Catalent employee. The primary duty of the **Associate Director, Regulatory Affairs** is to support regulatory strategy for product ... committed to a Patient First culture through excellence in quality and compliance, and to the safety of every...sites to ensure compliance with GMP regulations and to support preparation and filing of regulatory submissions… more
    Catalent Pharma Solutions (05/03/24)
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  • Director, Business Development - Regulatory

    Cardinal Health (Columbus, OH)
    …Discovery + Investigational New Drug Application + Label Expansion + State Licensing + Regulatory Training & Ongoing Support + Salvage Services Cardinal Health ... **Position Summary** For nearly five decades, Cardinal Health Regulatory Sciences' industry-trained regulatory consultants have provided expertise and guidance… more
    Cardinal Health (03/27/24)
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  • Director, Information Architecture (Hybrid)

    Merck (West Point, PA)
    …to design and implement data management systems, tools, and infrastructure to support biopharma research activities. + Identify opportunities for system ... pipeline. We are seeking a Senior Information Architect with expertise in biopharma research to support our organization's target and biomarker discovery,… more
    Merck (04/25/24)
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  • Associate Director - Quality Engineering…

    Lilly (Indianapolis, IN)
    …of Engineering and CSV will work across the POINT organization to provide Quality support to all Engineering activities and Computer Systems, including oversight ... life better for people around the world. **About POINT Biopharma :** POINT Biopharma Global Inc. is a...Lilly and Company. **Position Summary:** The Associate Director of Quality Engineering and Computer System Validation (CSV) is responsible… more
    Lilly (03/16/24)
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  • Quality Assurance Supervisor

    Catalent Pharma Solutions (Philadelphia, PA)
    …compliance as pertains to Catalent SOPs, regulatory , and customer requirements + Support Corporate and local Quality policies and initiatives. Support ... hiring a QA Supervisor. The QA Supervisor will provide Quality Assurance support for the Quality...of materials at Catalent-Philadelphia. Assist in the enforcement of regulatory compliance through state, FDA, DEA, CDC, and USDA… more
    Catalent Pharma Solutions (04/13/24)
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  • Head of Quality - Maryland

    Catalent Pharma Solutions (Harmans, MD)
    … Control and is the most responsible person for batch disposition. The Head of Quality will provide project guidance and support while working with customers to ... as the site's primary contact (with both customers and regulatory agencies) for the site Quality Unit....growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to… more
    Catalent Pharma Solutions (03/23/24)
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  • Associate Quality Systems Specialist

    Randstad US (Rocklin, CA)
    …Specialist will be part of the Quality team and responsible for providing quality support for the site quality management system. This position ensures ... future products and current product and process improvements. The position may represent Quality on cross-functional teams to support business needs driving a… more
    Randstad US (04/11/24)
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  • Manager, Quality Operations

    PCI Pharma Services (Rockford, IL)
    …understanding of tasks, responsibilities, business goals, and customer demands. + Provide 24-hour support for Quality related issues either by phone or email. + ... improvement/harmonization initiatives across multiple facilities. + Ensure Performance Metrics (Safety/ Quality / Regulatory /Delivery), goals, and objectives are on track… more
    PCI Pharma Services (02/11/24)
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  • Director, Quality

    Catalent Pharma Solutions (Philadelphia, PA)
    …and sustain a robust and effective quality system that delivers reliable, high- quality products that meet all customer and regulatory agency requirements and ... Quality is responsible for providing leadership and Quality Management support within each of the...guidance to the Quality Disposition, Materials Sampling Quality Assurance, Regulatory and Compliance Quality more
    Catalent Pharma Solutions (04/09/24)
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  • Sr. Manager / Associate Director Quality

    Kelly Services (Burlington, MA)
    …10-15% annual bonus** **Candidate Role:** We are seeking an experienced QA professional to support and evolve the quality management systems and processes at our ... **Sr. Manager/ Associate Director - Quality Assurance** **Burlington, MA** **Direct Hire** **Compensation: $125k-165k...US. + Lead and participate in third party and regulatory audits including preparation and responses. + Oversee qualification… more
    Kelly Services (04/04/24)
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  • Quality Control Analyst I

    Randstad US (Fort Worth, TX)
    …+ Write or revise standard quality control operating procedures. + Supply quality control data necessary for regulatory submissions. + Receive and inspect ... quality control analyst i. + fort worth ,...hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve… more
    Randstad US (04/20/24)
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  • Executive Director, Operations - GMP Lab

    ThermoFisher Scientific (Middleton, WI)
    …digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities ... our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. **Discover Impactful Work** The **Executive… more
    ThermoFisher Scientific (05/04/24)
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