68 Pharmaceutical Management Jobs in Billerica, MA
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Associate Director of Quality Kelly Science, Engineering, Technology & Telecom - Burlington, MA, United States such as SOPs and work instructions. · Oversee and develop CAPA, deviation, risk analysis and change control management. · Communicate with domestic and international pharmaceutical and life science customers 4 days ago
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Senior Clinical Trial Associate ONO PHARMA USA - Cambridge, MA, United States of clinical trial management experience in the pharmaceutical/biotechnology industries, or with a Clinical Research Organizations (CROs) or a clinical research site 1+ years of Clinical Operations work 9 days ago
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Quality Assurance Associate I Cambridge Isotope Laboratories, Inc. - Tewksbury, Massachusetts for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components in a GMP/ISO Environment. Responsibilities Maintenance and management of CIL’s change control 5 days ago
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Drug Discovery Lead – Solid and Heme Tumor Targeted Therapies (R0123711) Takeda - Cambridge, MA, United States expert and identified as a global Takeda thought leader Education & Competencies Advanced degree in health or life sciences (e.g., Ph.D., M.D., D.V.M.) with 15 years industry and 15 years management 3 days ago
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Director of Quality Assurance Harba Solutions Inc. - Boston, MA, United States . Qualifications: Bachelor’s degree with a minimum of 14 years of experience in a biotech or pharmaceutical regulated industry (including at least 10 years in Quality and 8 years in personnel management). Leadership Yesterday
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Associate Director- Clinical Trial Management (Oncology) at Regeneron Pharmaceuticals Regeneron Pharmaceuticals - Cambridge, Massachusetts for this role,** you must have at least a BS/BA/RN in science or a health-related field and 6-8+ years of relevant clinical study management experience. Biotech/pharmaceutical industry or contract research 11 days ago
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Director Quality Operations Vericel® Corporation - Cambridge, MA, United States , and honestly in our dealings and exercising sound judgment in performing our jobs. Basic Qualifications: Bachelor’s degree with a minimum of 14 years of experience in a biotech or pharmaceutical regulated 4 days ago
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***Sr. Clinical Programmer Analyst || 100% Remote*** Vaco - Boston, MA, United States and presentation skills Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical 8 days ago
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Senior Clinical Project Manager Novo Nordisk - Lexington, MA Independently manage interactions with clinical monitors, data management, safety, regulatory, pharmaceutical science and QA team members, both internally and externally Participate in the development of tools 3 days ago
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Director Clinical Operations EPM Scientific - Boston, MA, United States in clinical operations management within the pharmaceutical or biotechnology industry. Demonstrated leadership experience with a track record of successfully leading and managing clinical operations teams 5 days ago
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