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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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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.
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The Vice President of Business Development will engage with pharmaceutical companies and hospitals to commercialize Pear Bio’s precision medicine platform and drug discovery pipeline. Strong network in oncology and/or immuno-oncology therapeutics development, particularly with medium-large pharmaceutical companies.
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Key Experience and Requirements: BS/MS/PhD degree in a Pharmaceutical Manufacturing/Engineering, Analytical Chemistry, Chemistry, or related Quality fields. Team Development: Build and lead an empowered team of quality and regulatory experts, overseeing tools, business processes, and procedures supporting cell-based bioassay, cell & gene therapy, and virology testing.
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We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. This is an exciting opportunity to join our Digital and Cloud Team to help leading pharmaceutical and biotech companies adopt cutting edge scientific R&D technology.
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Experience preferable in pharmaceutical R&D setting with knowledge of the drug discovery process and the practice of laboratory animal medicine. In depth knowledge of regulatory requirements in working with research animals, experience in laboratory animal medicine and science, animal husbandry and vivarium operations.
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Skills & Requirements:A minimum of 2 years of experience in a pharmaceutical industry setting within Drug safety, Pharmacovigilance, or equivalent. 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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Candidate is required to have a broad functional knowledge of pharmaceutical sciences /the biopharmaceutical industry, with a clear understanding of drug development/commercial manufacturing of biopharmaceuticals as it relates to CGT products.
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Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions.
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The Patent Attorney/Agent will be responsible for client counseling on patent strategy and prosecution, drafting new patent applications in medicinal, pharmaceutical small molecule and polymers.
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Medical and Scientific Affairs serves a critical internal leadership and customer-facing support role, including pre- and post-market partnership to functions such as product management, sales and marketing, R&D, Clinical Affairs, Regulatory Affairs, Quality Assurance, Innovation, Strategy, Pharmaceutical Partnerships (Companion Diagnostics), and Technical Support.
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Experience with laws, regulations and industry guidance that affect the pharmaceutical industry including, but not limited to, FCPA, SFO, OIG, IFPMA, PhRMA & EFPIA guidelines, healthcare standard operating procedures, regulations governing drug and medical devices, anti-bribery laws, and state price reporting statute.
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BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. The Medical Support Specialist (Plasma Center Nurse) works under the guidance of the Center Manager (or Assistant Manager as applicable) for operational guidance and under the management of the Center Physician for medical issues.
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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.
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pharmaceutical job Company: Genoskin in Saugus, MA
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