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Experience working in biopharma, cell therapy, Good Manufacturing Practice (GMP), FDA regulated, or other regulated environments is a plus. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
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Experience in the Pharma/Biopharma required, cell therapy industry is plus. The Senior Manager, Validation, Engineering and Technology is responsible for supporting the production of personalized cell therapy products for both global clinical trials and commercial supply at the Bristol Myers Squibb Manufacturing Plant (Jump), Bothell, WA. The Senior Manager oversees the Right to Operate, Operational Excellence and Ongoing Monitoring area within the Validation, Engineering & Technology (VET) team.
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The Senior Manager will also oversee ad hoc teams performing VET activities, ensures the completion of all deliverables and develops the long term strategy of VET. Work will heavily involve the use and management of validation document control and quality system software and applications (e.g. ValGenesis, Infinity, Veeva Vault, Success Factors, BMRAM etc.
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Minimum of 15 years' experience in multinational pharma/biopharma organizations, covering Broad knowledge and experience with quality assurance and quality system, quality operations, regulatory compliance and understanding of current international regulatory requirements and trends for the manufacturing of API, DS and DP and advance therapies.
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Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
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10+ years of relevant BioPharma experience with a strong foundation in scientific communications. Stay up-to-date on emerging biopharma R&D and communications trends, monitoring peers, analyst reports and sentiment, and industry news; apply advanced concepts and principles to perform research, information gathering and analysis to prepare frameworks, innovative ideas, slides, and background materials.
$191,300 - $318,800 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Avantor's Lab and Production Services team is a crucial part of the Avantor Services group serving over 500 customers in biopharma, pharmaceutical, educational, industrial, and high-tech industries with customizable, flexible solutions and end-to-end laboratory operations support.
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Build and maintain a network of business development professionals across the pharmaceutical and biopharma industries. SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. Our mission is to revolutionize cancer treatment by developing breakthrough-therapeutic multi-specific antibodies and ADCs. With multiple assets in clinical trials and a robust preclinical pipeline, we are committed to advancing innovative therapies from discovery through IND-enabling stages.
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The Senior HR Generalist plays a critical role in supporting the human resources functions of our biopharma company in the Seattle area. Medical plans are currently provided through Premera Blue Cross.
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