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The primary function of the Associate Director/Director of Biologics CMC Regulatory Affairs is leading the development and implementation of biologics CMC global regulatory strategies for FDA, USDA and other agency regulated programs in development and registration preparation for biologics animal health pipeline programs.
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Proficient experience in crisis communications, corporate affairs, social content creation, media buying across social channels, social strategy development and influencer marketing. Support overall corporate communications team and objectives in various areas including public relations, social media, community affairs, internal communications and crisis communications.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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The Grad Intern works to support the Assistant Dean of Student Affairs by assisting with divisional programming initiatives, facilitating a variety of co-curricular learning experiences, and creating informational and educational marketing campaigns in partnership with the Office of Health Services, and Residence Life (approximately 30 hours/week.
InternExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Executive Office of Energy and Environmental Affairs (EOEEA) serves Commonwealth residents interested in outdoor recreational activities, clean energy solutions and those who work with animals and livestock.
$75,508.16 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Attends weekly Residence Life staff meetings; Student Affairs divisional meetings; hearing officer meetings; on-call meetings; and any other meeting pertinent to the position and/or position responsibilities.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The CDO is directly responsible for the Clinical Development and Regulatory Affairs teams and works in partnership with the Chief Technology Officer for CMC development and manufacturing related regulatory activities.
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The CDO supervises the Clinical and Regulatory Affairs teams and assists the President in defined areas including strategy, regulatory responsibilities, and communications. Lead the Clinical Development and Regulatory Affairs teams to ensure pre-clinical, pilot and pivotal effectiveness and target animal safety studies are executed to a high quality and in accordance with approved Plans, internal Quality standards, regulatory guidance and legal requirements.
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Reporting to the SVP of Q&R, the Senior Regulatory Affairs Specialist will have responsibility for; The Senior Regulatory Affairs Specialist will support and carry out the regulatory strategy and other regulatory aspects of product development and processes for the Biofourmis pharma partnerships and DTx algorithms.
$130,000 a yearFull-timeExpandUpdated 9 days ago - UpvoteDownvoteShare Job
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Job Title: Regulatory Affairs Specialist. Minimum of 8 years progressive regulatory affairs experience in medical device or pharmaceutical industry. Works with a team of regulatory affairs professionals to ensure the establishment of best practices within the assigned area of responsibility.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Job Segment: Surgery, Regulatory Affairs, Compliance, HR Manager, Human Resources Director, Healthcare, Legal, Human Resources. This role reports directly to the Vice President of Human Resources for the Endoscopy division and will support R&D, Medical Affairs, Clinical, Regulatory Affairs, and Finance functions.
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Principal Regulatory Affairs Specialist – Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Provide support for the Quality Assurance and Regulatory Affairs processes that the team adheres to. The Client Qualification Services Calibration Engineer works within the area of Metrology. The role will support with the management of Client’ s calibration and metrology program.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Experience in Medical and/or Regulatory Affairs. This position reports to the Myeloid Medical Promotional Review lead and is a key member of the US Medical Affairs Myeloid Team. The primary responsibility is to support the strategic review of promotional materials from a medical lens for Client products.
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Candidate must have experience in the development and implementation of health informatics solutions and clinical decision support (CDS) tools, the senior health systems specialist should be intimately familiar with the Department of Veterans Affairs historic electronic health record, VistA/CPRS (Computerized Patient Record System.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We are seeking a highly skilled Lead Director of FP&A to directly support the Medical Affairs organization globally. Certified Corporate FP&A Professional (FPAC) or Certified Public Accountant (CPA) or Certified Management Account (CMA.
$231,540 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago
affairs job in Framingham, MA
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