Hi this is Alekya B and I am a Resource Professional with Freyr Solutions ( ).Our Client is currently looking to hire a suitable candidate at Rahway, NJ for the following position and based on your pr...
read moreCompetencies Required:Seeking R&D background experience along with the Regulatory Affairs background. S with >10 years relevant industry experience in related R&D sciences discipline (engineering, che...
read moreDemonstrated expertise in FDA regulatory requirements and promotional content compliance. Proactive approach to identifying regulatory trends and implications for product innovation. We are an innovat...
read moreDemonstrated expertise in FDA regulatory requirements and promotional content compliance. Proactive approach to identifying regulatory trends and implications for product innovation. We are an innovat...
read moreCompetencies Required:Seeking R&D background experience along with the Regulatory Affairs background. S with >10 years relevant industry experience in related R&D sciences discipline (engineering, che...
read moreThe Senior Regulatory Affairs Specialist collaborates closely with their team, management, and provides leadership and mentorship to Regulatory Affairs Specialists 1 and 2. Reporting to the Regulatory...
read moreThe Senior Regulatory Affairs Specialist collaborates closely with their team, management, and provides leadership and mentorship to Regulatory Affairs Specialists 1 and 2. The Senior Regulatory Affai...
read moreTechnology Regulatory Affairs Specialist.
Technology Regulatory Affairs Specialist. We are seeking a dynamic and detail-oriented Technology Regulatory Affairs Specialist. Our client, a major bank in New York City, is looking for talented Tech...
read moreOur Senior Regulatory Affairs Specialist position is primarily focused on maintaining continued market access of our existing product portfolio, in addition to opportunities to provide regulatory supp...
read moreThe Regulatory Affairs Specialist will support the Director of Regulatory Affairs and collaborate with various departments to complete international product registrations (Canada, Southeast Asia, Midd...
read moreThe Regulatory Affairs Specialist will support the Director of Regulatory Affairs and collaborate with various departments to complete international product registrations (Canada, Southeast Asia, Midd...
read moreThe Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs. Implements regulatory activities such as obtaining global regulatory clearances and/or appro...
read moreThe Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...
read moreThe Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...
read moreSupport daily Regulatory Affairs function eg; compliance to CFR ,, ISO requirements, Company policies, operating procedures, processes, promotional task assignments into windchill and assigned trainin...
read moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Provide strategic input and technical guidance on regulatory requirements to development teams. Provide regulato...
read moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Compile, prepare, and review regulatory submission to US and EU. Utilize technical regulatory skills to propose ...
read moreRegulatory Affairs or equivalent industry experience is required. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's prod...
read moreThis position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...
read moreThis position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...
read moreEligibilities & qualifications.
Eligibilities & qualifications.
Working knowledge of relevant federal and state regulatory programs (e.
Working knowledge of relevant federal and state regulatory programs (e.
Develop regulatory strategies for new products with the guidance of Regulatory Management. Must make a proactive contribution to the overall Regulatory affairs department growth. Determine appropriate...
read moreDetermine appropriate regulatory requirements and strategies for new product development projects including both domestic and foreign activities and provide regulatory consultation to other internal a...
read moreThe Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Assisting in gatherin...
read moreThe Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. OTC regulatory experi...
read morePrepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance. Support regulatory filing submissions with the USDA for both dom...
read moreRegulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...
read moreRegulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...
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