Our 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 moreCooperSurgical is at the forefront of d Regulatory Affairs, Specialist, Regulatory, Healthcare, Manufacturing, Surgical.
Our 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 moreCooperSurgical is at the forefront of d Regulatory Affairs, Specialist, Regulatory, Healthcare, Manufacturing, Surgical.
Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...
read moreIntegration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...
read moreThe requirement is for 3 Regulatory Affairs Specialist. The candidates will work with client & Our client's teams to deliver best in-class solutions for regulatory submissions. Facilitate worldwide pr...
read moreThe requirement is for 3 Regulatory Affairs Specialist. The candidates will work with client & Our client's teams to deliver best in-class solutions for regulatory submissions. Facilitate worldwide pr...
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 moreRegulatory Affairs Project management experience. Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects a...
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 PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regula...
read moreThe PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regula...
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 moreProvide consultation and advice to regulatory specialists regarding change control and product development. Contribute to continuous improvement initiatives within the regulatory affairs function. Off...
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 morePerforms quality control, research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring that Good Clinical Practices (GCP) ...
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 moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input ...
read moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input ...
read moreProvides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's products and processes. Knowledge in relevant Regulatory Affairs areas...
read moreMaintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within th...
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.
The 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 moreRegulatory Affairs Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be res...
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 Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be res...
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...
read moreDevelop appropriate awareness and training programs for TSMs consistent with regulatory compliance policies and procedures. Conduct routine Regulatory audits of Henry Schein facilities, affiliates and...
read moreThis role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Stra...
read moreAt least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. T...
read moreRegulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies,...
read moreReviews and assesses proposals to regulatory authorities on regulatory paths and clinical plans. Applicants with educational backgrounds in Regulatory Affairs or related Health Care Management Degrees...
read moreApplicants with educational backgrounds in Regulatory Affairs or related Health Care Management Degrees are preferred. Analyzes and communicate the adequacy of proposed regulatory pathways and strateg...
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