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The Regulatory Affairs Specialist is responsible for preparing Nutritional Facts and Ingredient Statements (reg sheets) for all products within the Bimbo Bakeries USA (BBU) organization, including private label brands and foodservice.
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Leidos QTC Health Services is seeking a Medical Quality Assurance (QA) Specialist to support our Veteran Affairs Operations in Philadelphia, PA. Foreign Medical Graduate or better. Additional factors considered in extending an offer include (but are not limited to): geographic location, responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
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The role involves close partnership with project Clinical Scientists and extensive collaboration with colleagues across disciplines, including Discovery, Translational Science & Medicine, Clinical Pharmacology, Biostatistics, Data Science, Medical writing, Clinical Operations, Global Medical Safety, Regulatory Affairs, Quality, Medical Affairs, Commercial and Market Access.
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The scope of responsibility spans drug discovery and development, medical affairs, marketing and brand management, sales, managed markets, manufacturing operations, trade and distribution, and finance.
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Target Buyers: Clinical Operations, Regulatory Affairs, Medical Affairs, Real World Evidence, Real World Data Owners, Medical Operations, Outcomes Research, Health Economics. Target Buyers: Drug Safety, Pharmacovigilance, Regulatory Affairs, Medical Operations.
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Primary Location NUS-Pennsylvania-Horsham Other Locations NUnited States Organization Janssen Scientific Affairs, LLC (6120) Job Function Medical Science Liaison. Job Description Janssen Scientific Affairs, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Field Director, Lung Oncology, to cover the Northeastern United States territory.
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ClinChoice is a global CRO supporting data management, biostatistics, statistical programming, clinical operations, regulatory affairs, safety, pharmacovigilance, toxicology, medical affairs, medical writing, quality, risk, and compliance services to the pharmaceutical, biotechnology, and medical device industries worldwide.
Full-timeRemoteExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Opportunity for a scientist to join team in Varicella bulk vaccine manufacturing, within the Manufacturing Division, supporting a new PAT (process analytical technology) lab and laboratory operations.
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As a Signals Intelligence Analyst, you will intercept and analyze foreign communications; relay intelligence reports regarding combat, strategic, and tactical intelligence information; and study and locate radio signals to understand the tactics and organization of foreign military forces.
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Reporting to the Director in Regulatory Chemistry, Manufacturing & Controls (CMC), the Senior Scientist is responsible for implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned products in accordance with global regulations, guidance's, and defined regulatory strategies.
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License to practice Speech Language Pathology issued by PA Bureau of Professional and Occupational Affairs is preferred. Collect and analyze data for progress monitoring. Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program.
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AECOM is actively seeking an Entry Level Geologist or Environmental Scientist for employment in our Conshohocken PA office to support soil and groundwater investigations and remediation projects.
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Obtains and reviews clinical study data with Clinical Data Manager and other Clinical Affairs personnel, as needed for IDE and PMA reporting. The Regulatory Affairs Specialist drafts, submits and gains clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.
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This individual will work closely with multiple functions including Franchise Brand Marketing, Strategic Customer Group (SCG), Field Sales, Medical Affairs, Real World Value and Evidence, and external partners in order to effectively develop and deliver on key access strategies and goals.
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B) Global Regulatory Affairs and Clinical Safety : Focus on late-stage and lifecycle drug activities, understand key regulatory policies and the procedures for interacting with health agencies (e.g. FDA); understand key elements in pharmacovigilance, drug safety monitoring, signal detection and processing of adverse reports After a successful first year, the Physician Scientist will be equipped to assume a leading role in the team with additional responsibilities and interactions.
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foreign affairs jobs Title: data scientist in North Wales, PA
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