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Master’s degree in Biotechnology, Regulatory Science, Pharmaceutics or Pharmaceutical Science or Industrial Pharmacy (or its foreign equivalent); plus 6+ years of quality assurance experience within the pharmaceutical drug development industry as a Quality Assurance Manager, Lead, Specialist or Associate.
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1-5 years of patent prosecution experience in a biotechnology practice. Life Sciences Associate Attorney will be responsible for providing legal counsel and support on patent prosecution and counseling projects within the life sciences sector, particularly focusing on emerging companies involved in antibodies, DNA or RNA therapeutics, chemical biology, gene-editing, and related areas.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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We believe that you are a Medical Doctor with specialty clinical training in endocrinology, or obesity medicine, who has well-established clinical expertise in the treatment of metabolic disorders with a minimum of 7-10 years of clinical research experience, either in the academic research environment or in the pharmaceutical/biotechnology industry.
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Collaborate closely with other groups within the early CVRM therapeutic area to provide expert clinical input into pre-clinical scientific activities such as target selection, lead generation and optimization, clinical pharmacology, in vivo animal studies, in vitro studies, and drug formulation and manufacturing.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The candidate is also expected to support outsourcing efforts for designing, monitoring, execution and reporting of the nonclinical toxicology studies, have experience in managing regulatory-compliant toxicology studies in a CRO or biotechnology/pharmaceutical company, and have demonstrated understanding of GLP compliance and the relevant ICH & FDA guidance documents.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Senior Analyst has over a decade of professional experience with a focus on biopharmaceutical, including biotechnology equity research analyst at Jefferies, strategy consultant at a leading consulting firm, investment profession at private equity and venture capital funds, and marketing/sales management at a major medical device company.
$135,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Five years minimum experience in the clinical laboratory or biotechnology with strong background in blood bank/hematology and marrow/stem cell manufacturing and experience and/or extensive knowledge in quality assurance/improvement, regulations and compliance.
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To meet the stringent needs of biotechnology research and production customers, the company's cell culture sera and bioprocess liquid manufacturing facilities are segregated between animal origin-free cGMP manufacturing and animal component cGMP manufacturing.
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Minimum of 7-10 years of relevant document control experience in the biotechnology or pharmaceutical industry or in a manufacturing setting; hands-on experience with vQV or equivalent electronic document management system.
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A minimum of 10 years of experience in clinical pharmacology within the pharmaceutical or biotechnology industry, with significant experience in antibody development. Collaborate closely with cross-functional teams, including clinical development, non-clinical development, DMPK, regulatory affairs, and clinical operations, to ensure alignment and integration of clinical pharmacology principles throughout the drug development process.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. We're looking for an Instrumentation and Controls Engineer , working in Pharmaceuticals and Medical Products industry in 500 Soldiers Field Road, Boston, Massachusetts, 02134, United States.
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LI-AR1 LI-Hybrid Company Information Vertex is a global biotechnology company that invests in scientific innovation. Knowledge and Skills: Expert knowledge of global GMP requirements governing CGT products Ability to evaluate quality matters and make decisions utilizing risk-based approach Strong technical knowledge including but not limited to: QMS, risk management, change control and governance.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Minimum 10 years regulatory operations experience in a biotechnology or pharmaceutical environment with demonstrated ability to present and articulate requirements. Reporting to the Head of Regulatory Affairs, the Director, Regulatory Operations is responsible for the management and oversight of regulatory submissions, systems, and associated procedures.
$216,090 - $238,309 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. In this new role, you will manage clinical trial(s) under the leadership of the VP, Clinical Operations clinical development team.
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Laboratory responsibilities may include Biology, Microbiology, Anatomy & Physiology, Chemistry, General Science, Energy, Nutrition, Biotechnology, or Physics classes. Bachelor's degree in Biology, Biotechnology, Chemistry, Microbiology, or closely related field; with one (1) year experience and/or training involving laboratory operations; or an equivalent combination of education, training and experience.
ExpandApply NowActive JobUpdated 7 days ago
biotechnology job in Lynn, MA
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