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Complies with all laws, regulations, and policies that govern the conduct of BMS. Required Qualifications & Experience- Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.
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Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. 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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Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 8 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, Master's degree in above areas with 6 years of experience in a pharmaceutical/biotech QC laboratory.
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We are hiring for a QA Director to join a nonclinical CRO working with both small and large animal models while working collaboratively with groups that span biotechnology research. Terminal degree (DVM, PhD, MD) in pharmaceutical, biological, or chemical sciences.
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Position SummaryThe 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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Proven track record of leadership in computational biology or bioinformatics in a pharmaceutical, biotechnology, or academic setting. Experience working in the pharmaceutical or biotechnology industry, particularly in the context of drug discovery.
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Position Summary:ultrafocused – Work together to fearlessly uncover new possibilitiesReporting to the Head of Global Planning, Ultragenyx is seeking a highly motivated Associate Director, Clinical Supply Gene Therapy with expertise in end-to-end pharmaceutical clinical supply strategies and operations.
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5 to 7 years of in-depth knowledge and clinical development experience within the pharmaceutical or biotechnology industry, or 7 to 9 years clinical trial experience in an academic setting, collaborating with pharmaceutical sponsors.
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DPS Group is a global EPCMV firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries.
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2+ yeas of document control/document management experience working in an FDA regulated industry (biotechnology, pharmaceutical, medical device, etc. Strong experience working with Electronic Document Management Systems (EDMS) such as Master Control, Veeva, Agile.
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Nemera is a world leader in the design, development, and manufacturing of drug delivery devices for the pharmaceutical, biotechnology, & generics industries. Assess results of Customer Complaint investigations and Corrective Actions for application, validity and conformance to FDA regulatory, QSR, ISO and Customer requirements.
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The position demands a seasoned professional with a robust background in managing substantial capital projects within the pharmaceutical industry, specifically those involving comprehensive Good Manufacturing Practice (cGMP) standards.
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Our products and platforms have attracted multiple partnerships with leading pharmaceutical and biotechnology companies around the globe. MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies.
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Proclinical is seeking a Senior Regulatory Affairs Associate or a Regulatory Affairs Consultant with a strong background in CMC post-approval. Update HA question record in Vault and coordinate dispatch of information to Affiliate noting status changes in Veeva.
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