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The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.
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The candidate will be responsible for conducting equipment inspections for chemical, pharmaceutical/biopharma, fertilizer, petrochemical , and power generation plant to gather relevant information on.
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Externally, this position maintains relationships with medical and clinical operations decision-makers at pharmaceutical, biopharma, biotech and medical device companies. Externally, this position maintains relationships with medical and clinical operations decision-makers at pharmaceutical, biopharma, biotech and medical device companies.
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For more details, refer to InSite BMS Website/ People and Performance/BMS BioPharma Behaviors. The qualified candidate demonstrates characteristics of our BMS BioPharma Behaviors. BMS Biopharma Behaviors.
$43 - $47 a yearExpandUpdated 8 days ago - UpvoteDownvoteShare Job
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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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At least several years relevant work experience, in the Life Science industry, ideally with prior project management or consulting experience (e.g., associate or project management roles in Life Science Consulting or at a Pharmaceutical, Medical Device, or other Biotech/Biopharma Company.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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Provides Quality Assurance support for GMP Raw Materials that support the production of GMP Manufacturing operations of cell therapy products at our US Cell Therapy facility located in Princeton, NJ. Responsibilities include providing QA oversight of materials used for Manufacturing, Quality Control, and Process & Analytical Development.
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The Specialist, Quality Assurance provides Quality Assurance support for GMP Raw Materials that support the production of GMP Manufacturing operations of cell therapy products at our US Cell Therapy facility located in Princeton, NJ. Responsibilities include providing QA oversight of materials used for Manufacturing, Quality Control, and Process & Analytical Development.
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Expected client engagement is face-to-face with expectations of travel. Opportunities for career development with on-the-job training, certification assistance and continuing education reimbursement. We deliver transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those performing clinical trials.
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Strong communication skills allowing the candidate to serve as a primary point of contact for communications across the groups (Biopharma IT, Business teams and any third party involved in the Project or Program), effectively communicating relevant information to key stakeholders as per the defined Communications plan.
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Experience in the manufacture of drug substance and/or drug product or quality control laboratories is desired Biopharma Behaviors. For more details, refer to InSite Website/ People and Performance/ BioPharma Behaviors.
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Further guidance on physical activities, requirements, visual acuity, and working conditions is available in HCM. Tasks, duties, and responsibilities as listed in this job description are not exhaustive.
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Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Lead team supporting Quality Management Systems (QMS) with QA review and decisions on; CAPAs, Change Controls, Customer Complaints, operational deviations, and Self-Inspection as needed.
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Coordinate with leaders and SME’s across the organization to create compelling and goal-driven solutions for clients and prospects, and ensure tactical and strategic company goals are achieved. Executive level client penetration and development experience is essential.
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biopharma job Company: Genesis Research in Dayton, NJ
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