11 Pharmaceutical Regulatory Compliance Jobs in Billerica, MA
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Senior Clinical Trial Associate ONO PHARMA USA - Cambridge, MA, United States of the Pharmaceutical Industry Clinical trial process (clinical trial conduct, documentation and reporting) in accordance with ICH/GCP and other regulatory compliance guidelines. Cognitive Skills Problem solving 22 days ago
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Director of Quality Assurance Albion Rye Associates - Boston, MA, United States regulatory requirements is a plus Solid well-grounded experience in GXP compliance including knowledge and experience in preparation of Clinical sections of INDs, CTAs, BLAs, MAAs and NDSs submissions 22 days ago
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Director of Clinical Operations Global Life Science Hub - Boston, Massachusetts and collaborations. Collaborate closely with Quality Management to ensure ongoing compliance and regulatory adherence. Qualifications: Bachelor's degree in life sciences or related field; advanced degree preferred. 10 3 days ago
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Senior Director, Global Medical Affairs, ATTR Cambridge, MA to inspire a matrix team to excel by fostering a climate of energy, excitement and personal accountability. Current working knowledge of legal, regulatory, and compliance regulations and guidelines. Ability 17 days ago
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Medical Science Liaison Incyte Corporation - Boston, Massachusetts, USA hematology/oncology experience is strongly preferred. Clinical research experience is preferred. Knowledge of applicable treatment, compliance, and regulatory guidelines. Excellent interpersonal communication 23 days ago
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Medical Science Liaison, New York City/ Boston, MA Boston, MA hematology/oncology experience is strongly preferred. Clinical research experience is preferred. Knowledge of applicable treatment, compliance, and regulatory guidelines. Excellent interpersonal communication 20 days ago
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Senior Quality Assurance Consultant LS Solutions - Cambridge, MA in quality assurance and regulatory compliance in the pharmaceutical and medical device sectors. Expertise in cell therapy manufacturing, cloud-based data management systems, and medical device remediation More than 30 days ago
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Associate Director, GMP Quality Control Sumitovant Biopharma - Marlborough, MA, US changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed. Responsible for compliance with regulatory filings and therefore must have experience More than 30 days ago
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Medicinal Chemist Convergence Therapeutics - Cambridge, United States , results, and data analysis in compliance with regulatory requirements and company SOPs. * Provide technical expertise, troubleshooting support, and training to junior scientists and team members as needed More than 30 days ago
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Qulaity Manager - Medical Devices - ISO 13485:2016, Kaizen CyberCoders - Beverly, MA , and systems. Ensure compliance with applicable FDA, CE, and other regulatory requirements. Qualifications: Minimum 5 years of experience in Quality roles in a medical device/pharmaceutical industry 90,000.00 - $130,000.00 28 days ago
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