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Job Duties Support the VP of Global Regulatory Affairs Operations in strategic planning and execution. The Operations Manager will work directly with the VP of Global Regulatory Affairs Operations to ensure the smooth and efficient delivery of QARA programs and goals.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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License to practice Speech Language Pathology issued by PA Bureau of Professional and Occupational Affairs is preferred. Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program.
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Organizational Relationships: (1) Responsible to the Associate Dean, Student Services, Pocono for assigned responsibilities (2) Work closely will all departments of Student Affairs in carrying out responsibilities (3) Relates role to the mission and goals of department and college community, (4) Accept other responsibilities as assigned.
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The Senior Manager, Professional Strategy will help create and deploy strategic plans to cultivate solid relationships with Key Opinion Leaders (KOLs), key accounts, educational institutions, and professional associations, in support of the Bausch & Lomb Pharmaceutical business.
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This position is located in the Division for Ocean Affairs and the Law of the Sea of the Office of Legal Affairs (OLA). Register on the United Nations careers website and complete your job application.
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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
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Ensures content voice, tone, and style; serves as a writer, editor, and content optimization expert across multiple internal/external channels to support marketing, communications, and public affairs goals.
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Responsible for management of the delivery of legal services to support, globally, business operations and functional areas for Medical & Scientific Affairs (MSA) and Quality Assurance & Regulatory Affairs (QARA) activities.
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Represents the US medical affairs perspective at the Global Medical Team and Medicine Commercialization Team meetings, bringing a strong US view on medical strategy and US customer needs as input to global strategy; Cocreates Global Medical Strategy to ensure US needs and issues are addressed.
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May oversee and direct the work of other Regulatory Affairs professionals. Serves as a regulatory liaison for new product development and make regulatory assessments of proposed changes to existing products for impact to regulatory documentation.
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Creates and obtains approval for an annual comprehensive marketing plan including promotional materials, medical conferences, scientific affairs initiatives, website, email, and digital marketing campaigns.
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Legal & Regulatory, Area Managers, Vice President Sales. Works closely with Legal, Regulatory and Scientific groups to ensure promotional materials meet compliance standards. Skilled at successfully navigating medical, legal, and regulatory review process.
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Manage communications with the US FDA, Health Canada, notified bodies and other regulatory agencies/authorities. Conduct regulatory research. B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry.
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Proficient in identifying sustainable solutions, implementing eco-friendly practices, and driving organizational change towards environmental stewardship, social responsibility, recycling, and economic viability for a resilient and sustainable future.
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affairs job Title: regulatory affairs Company: Beigene in Bethlehem, PA
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