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10-12 years of quality assurance and regulatory compliance experience within the biotech or pharmaceutical industry. Oversee quality vendors responsible for GXP audits, compliance, and GMP batch record review.
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Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Bachelor degree or 10+ years of GMP QC laboratory or biotech/pharmaceutical industry experience.
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Prior internship experience in quality assurance within the biotechnology or pharmaceutical industry is highly desirable. Batch Record Review: Review and analyze batch records for adherence to Good Manufacturing Practices (GMP) and internal quality standards.
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12+ years of experience in the Biotechnology/Pharmaceutical industry with a minimum of 7 years of experience in cGMP manufacturing operations. Progressive experience in a leadership role in pharmaceutical development and commercial manufacturing; experience partnering with CMOs required.
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A minimum 3-5 years' experience in an FP&A role/Finance operations role, preferably in the biotech/pharmaceutical industry. Experience with data manipulation and visualization tools is a plus (Alteryx, Tableau and Microsoft Power BI.
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By leveraging our proprietary DiversImmune® and MultiMabTM antibody discovery and engineering platforms, Abpro is advancing a pipeline of antibodies to treat cancer, eye, autoimmune, and infectious diseases, both independently and through collaborations with global pharmaceutical and research institutions.
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Role Summary:The Sr. Specialist, Quality Management (GLP) applies working knowledge in pharmaceutical research and quality assurance to provide consultation to pre-clinical development teams and performs independent quality audits of pre-clinical vendors and internal processes and systems.
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We do this by supporting pharmaceutical clients in Patient-Centered Outcomes research. Who we are: Adelphi Values (part of Omnicom Health Group) is a leading health outcomes consultancy that works with a wide range of pharmaceutical companies.
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Minimum 5 years selling into Medical Device and or Pharmaceutical/Biotech Manufacturing Companies. Focused on composable, human-centric solutions for industrial environments, Tulip is disrupting the MES category and has been recognized as a World Economic Forum Global Innovator.
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May perform the duties of a Security Officer in accord with post orders and company policy.
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We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
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The role is mainly responsible for supporting Flow Cytometry and FACS equipment and scientists' operators as requested by our pharmaceutical customer. We are looking for a highly motivated Instrument Support Specialist to provide critical, on-site, scientific and operational support as part of a dynamic PerkinElmer lab service team.
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Relevant experience includes work in blood banking, laboratory or a pharmaceutical manufacturing facility. Relevant experience includes work in blood banking, laboratory or a pharmaceutical manufacturing facility.
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We work with some of the largest professional services, consulting, hospitality, leisure retail, and pharmaceutical brands in the world including Circle K, Starbucks, BSH, Delivery Hero, Costa Coffee, The Boston Consulting Group, PwC, Novartis etc.
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Bachelor's degree in the Life Sciences with 7+ years in pharmaceutical or biotech drug development. The Sr Manager, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as varied vendors supporting Clinical Studies.
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pharmaceutical job in Cambridge, MA
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