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Title: Regulatory Affairs Associate - Data Entry. Work is performed under the general supervision of more senior Regulatory Affairs CMC Systems professionals. Title: Regulatory Affairs Associate - Data Entry.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Serving as a field resource for The Medical Affairs Company (TMAC), the Clinical Trial Liaison (CTL), reporting as Early Clinical Liaison , will represent the Company’s Respiratory Clinical Development program.
ExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Role: Regulatory Affairs Specialist. Working knowledge of relevant federal and state regulatory programs (e.g., FIFRA, TSCA, Prop 65). Advanced degree in environmental science, chemistry, toxicology, environmental engineering, or other applicable related degree.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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10+ years of Regulatory Affairs experience within a pharmaceutical or biotech setting. As the Regulatory Affairs Director, you will have the opportunity to lead Allogeneic trials – the most innovative in history.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations, Regulatory Affairs, Medical Affairs, and Pharmacovigilance. This position interacts cross-functionally with functional teams in Clinical Trials which include Clinical Operations, Regulatory, Pharmacovigilance, Medical Writing and Data Management to ensure compliance to the GCP Quality Management System and all applicable regulatory requirements.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Collaborate with Clinical Development (including PV/Safety), Regulatory Affairs, and Development Operations (including Clinical Operations, Data Management, and Biostatistics), CROs and clinical sites to support overall GCP compliance and inspection readiness.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Establish and operationalize policies, Standard Operating Procedures (SOPs), and quality assurance processes that ensure program compliance; partner with CRS Compliance and Regulatory Affairs Program to align with existing policies and systems.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Minimum of 10 years of progressive experience in quality assurance, regulatory affairs, or a related field within the pharmaceutical, over the counter (OTC), or dietary supplement industry.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Specialist will ensure global compliance with all cosmetic and OTC regulatory requirements by performing a wide range of tasks. Regulatory Affairs Specialist – Onsite - Ottawa, Illinois.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Ability to effectively communicate and collaborate with a wide range of partners, including IT, R&D, operations, regulatory affairs, and senior management. Deep Industry Knowledge and a thorough understanding of the biotech and pharma industries, including regulatory environments, R&D processes, manufacturing, supply chain, and market dynamics.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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10-12 years of experience in regulatory affairs in a cosmetic or personal care products company; additional experience in quality control is a plus. Manage and direct staff to regularly audit regulatory files and control documents such as SDS, COA, Spec, and Stability to ensure all information is accurate and up to date in preparation for any formal audits.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Regulatory Affairs Manager - Permanent - San Francisco Bay Area. Proclinical is seeking a Manager, Regulatory Affairs for a global medical device company. Responsible for developing and implementing global regulatory strategy and roadmaps through deep understanding of the competitive market landscape, regulatory / legislative initiatives, and product marketing strategy for product portfolio.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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They will actively participate in the development and management of the Regulatory Affairs (REG) department within the Value Delivery Centre (VDC) REG, in relation to the SPM and CMC Practice Areas.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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These areas of competence are complemented by an enhanced range of services for development and regulatory affairs, right through to approval of end-to-end medical products. The Environmental Health and Safety Manager ensures that Roechling Medical Rochester complies with local, state and federal environmental, health and safety regulations.
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regulatory affairs jobs in New Orleans, ID, Nevada
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