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We invested in new offices, sector teams and practice groups including investor engagement; shareholder activism; governance; regulatory and public affairs, including geopolitical; crisis; litigation; social issues including climate change and diversity, equity and inclusion; cybersecurity, data and privacy; employee engagement; digital communications; opinion research and analysis, and; creative services.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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This role will support all commercial legal and healthcare compliance aspects of Kite’s cell therapy business in the U.S., including support for Commercial, Medical Affairs, Regulatory, Market Access, and Government / Public Affairs.
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Dorsey is seeking a Regulatory Affairs Associate with four to six years of experience to join our Anchorage office. This associate will have the opportunity to work on a wide variety of issues and matters, including corporate and municipal governance, contracting, financings, real property, proxy and proxy statements, and annual meetings (parliamentarian and inspector of elections), in addition to commercial telecommunications and merger and acquisitions.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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We are seeking a highly motivated Regulatory Affairs and Quality Assurance (RA/ QA) experienced professional to join DermBiont. Knowledge of GLP and GCP, Pharmacovigilance (PV), ICH, FDA requirements and guidelines for small molecules, including drafting, interpreting, and implementing quality assurance policies and procedures for regulatory documents, as well as establishing document management activities.
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This position reports to the VP, Global Regulatory Affairs. Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Associate is responsible for assessing and ensuring regulatory compliance of the quality management system. We are looking for a Regulatory Affairs Associate to join our company full time in Conshohocken, PA. This position requires the incoming candidate to be onsite, 5 days per week at our office in Conshohocken.
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We are looking for an Associate Microbiologist to join our Food Safety Quality & Regulatory Affairs team in Omaha, Nebraska! As the Associate Microbiologist, reporting to a Senior Microbiologist, you will draw upon your education and experience in microbiology to analyze and study the general properties of bacteria and other microorganisms in both food and food processing environments through applied research and routine testing at the Corporate Microbiology Laboratory.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Role: Regulatory Affairs Associate. Role: Regulatory Affairs Associate. Proven successful track record of authoring/submission/approval of Class III implantable PMA supplements. Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Work closely with internal and external functions such as clinical development, medical affairs, CMC, global regulatory affairs, TGO, sourcing and commercial to seamlessly integrate technical process development activities into the overall working model.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Regulatory Affairs and Quality. Generous time off plus a Holiday shutdown week. Corporate Strategy & Business Development. With offices in Waltham and NYC and experts employed around the world, you will have the opportunity to learn from and collaborate with a select group of the brightest minds in pharmaceuticals and biotechnology.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Rocket Pharma is seeking an experienced and highly motivated Associate Director, Regulatory Affairs (USL f or AAV), who enjoys a fast paced, dynamic work environment at the forefront of innovation.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Under the general direction of the Provost and Vice President for Academic Affairs, the Associate Vice President (AVP) for Grants, Research, and Sponsored Programs (GRaSP) primarily focuses on collaboratively developing and implementing a strategic agenda to secure and manage extramural funding and elevating the profile of grant writing and scholarly activity.
$14,167 - $29,425 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Associate Director, CMC Regulatory Affairs is a hands-on and independent role requiring a strong individual who will provide strategic and operational support to multiple programs, with an emphasis on CMC (Chemistry, Manufacturing, and Controls.
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