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I have a talented group of recruiters who specifically source Technical Sales Professionals, Scientists, Regulatory Affairs, Scientific Affairs, Executive Technical professionals, Quality Assurance, Product Development, Technical Service, Nutrition, Analytical and Corporate Chefs.
$165,000 - $180,000ExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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The Executive Director of Regulatory Affairs is a product facing role that leads a designated part of the Inflammation and Rare Disease Global Regulatory Therapeutic Area in the Global Regulatory Affairs organization.
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Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st generation PMA submission as well as future supplements and OUS international registries for global commercialization.
RemoteExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Sr. Regulatory Affairs Specialist. · Must have a solid history and good practices working in regulatory affairs. 5+ years of regulatory experience in Beauty, preferably in color cosmetics, or personal care industry, including labeling, registrations, formulation/ ingredient compliance.
$80,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Head of Global Regulatory Affairs will also promote the priorities of the leadership team and other key business leaders at TCW. 3+ years of experience at a U.S. regulatory rule making agency (e.g., SEC, Fed, DOL) or trade organization covering financial services (e.g., ICI, IAA, IRI, SIFMA.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The Director, Regulatory Affairs is responsible for assisting with establishing and managing regulatory strategies, life cycle plans, and pre/post regulatory approvals. Establish regulatory strategies and process by collaborating and coordinating with relevant development and CMC team members.
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Team with business unit Regulatory Affairs Specialists (RAS) to provide regulatory support for new product introduction (NPI) and marketed products under MDD and MDR Regulation. As Principal Regulatory Affairs Specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum Qualifications: 8+ years professional experience as either a healthcare litigation, regulatory, or transactional associate in a nationally recognized law firm, in-house counsel at a nationally recognized company or organization, or a combination thereof.
$169,936 - $305,760 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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They are currently seeking a skilled regulatory professional to join their growing team as Director/ Sr. Director CMC Regulatory Affairs. 7-10yrs of direct Pharmaceutical experience within Regulatory Affairs.
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Cases will cover a wide range of challenging matters such as Environmental Resource Permitting challenges, Consumptive Use Permitting challenges, procurement bid protests, rule challenges, and regulatory enforcement cases.
$80,184 - $136,323.2 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum 8-10 years of combined regulatory affairs experience in color cosmetics, both in domestic and international markets. Strong knowledge and expertise in international regulatory affairs and packaging/labeling compliance.
$130,000 - $150,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Title: Regulatory Affairs Manager. In-depth knowledge of the Global Regulatory Affairs environment – Guidelines and legislation. · Broad understanding of the pharmaceutical business in general and of other relevant associated regulatory areas (e.g., Clinical Affairs, Medical Devices, Chemicals Regulations, etc.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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General understanding of drug development and pharmaceutical manufacturing from concept to launch including requirements for product development,manufacturing and marketing and the impact of regulatory changes on business goals/objectives.
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The Regulatory Affairs Specialist will be responsible for combining scientific, regulatory, and business issues to enable projects that are developed, manufactured, and distributed to meet local regulations and requirements.
$76,163 - $101,551 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Managing regulatory compliance activities for Kindeva and existing customer products and registrations as required and providing strategic planning for regulatory changes. Providing regulatory support to team members as required on specific project issues ensuring alignment with global guidelines and legislation and the specific business needs of Kindeva.
Full-timeExpandApply NowActive JobUpdated 1 month ago
Title: regulatory affairs in Los Angeles, CA
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