A company is looking for a Senior Associate Regulatory Information Management. ...
The Associate Director of Regulatory Innovation supports regulatory objectives for Allergan Aesthetics products including coordination, management of global submissions. Authors and supports regulatory submissions, regulatory operations, change control, lifecycle management, interactions with regula...
A company is looking for a Senior Associate Regulatory Affairs for a remote position. ...
This individual has responsibility for products/multiple driver indications for one or more products or projects within Global Regulatory Aesthetics Pharma and supports the Global Regulatory Lead (GRL, Director), in the development and execution of the regulatory strategy. Collaborates and liaisons ...
A company is looking for an Associate Regulatory Coordinator. ...
My client is working towards their first ever NDA and seeking an Associate Director/Director Regulatory Advertising and Promotions/Labeling to join their growing Regulatory team. Provide leadership for and manage regulatory aspects of the copy review / approval process for promotional materials; ens...
Collaborate closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Pharmacovigilance, and Quality Assurance, to support regulatory submissions and responses to regulatory agencies. They are seeking a highly skilled and experienced an Associate Director OR Director, ...
Assist Regulatory Manager in maintenance of customer regulatory files and raw material files. Obtain technical/regulatory documentation from raw material vendors. Helps manage regulatory compliance related to EU PIF/dossiers. Maintain regulatory files for each ingredient (TDS, SDS, CofA, ingredient ...
Work collaboratively to support the RA CMC team to meet deliverables and timelines by executing routine data entry, quality control of that data entry and associated reports. Work is performed under the general supervision of more senior Regulatory Affairs CMC Systems professionals. ...
CMC Regulatory Technical Writer, Associate Director/Director. CMC technical document review and writing, authoring and compiling the CMC sections for global regulatory filings by working closely with the cross-functional teams including CMC, Quality, Clinical and Regulatory Affairs to ensure all CMC...
Lead global CMC regulatory submission development - responsible for planning, coordinating, and developing high quality, compliant and timely CMC (Quality) regulatory submissions according to current regulatory requirements and guidance to obtain efficient and timely regulatory approvals (IND/IMPD, ...
Experience with regulatory submissions and maintaining regulatory documents. ...
Are you a skilled Controls Engineer ready to take your career to the next level? We're looking for a talented individual to join our dynamic team and contribute to the design, development, and implementation of PLC systems for custom machinery.If you're passionate about cutting-edge technology and t...
This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...
This is a rapidly growing high-tech entrepreneurial company in the heart of West Los Angeles.The Principal Research and Development (R&D) Engineer oversees and participates in the capture, planning, design, prototyping, and verification of wireless technology projects.Technical management of R&D pro...
Assist counsel with regulatory and internal reviews, including, but not limited to, coordinating e-Discovery collections, executing and analyzing transactional reports, conducting legal research, coordinating document productions, and preparation of regulatory responses. Support regulatory change ma...
This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...
Corporate/Regulatory Associate. Our corporate/commercial health practice offers general counsel, health regulatory and governance advice to healthcare organizations, associations and professionals. We provide strategic advice and regulatory opinions on a wide variety of issues. ...
This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...
Bachelor’s degree in Engineering, Physical or Biological Sciences, Regulatory, other technical disciplines, or equivalent. ...
This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...
Assist counsel with regulatory and internal reviews, including, but not limited to, coordinating e-Discovery collections, executing and analyzing transactional reports, conducting legal research, coordinating document productions, and preparation of regulatory responses. Support regulatory change ma...
This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...
This is a rapidly growing high-tech entrepreneurial company in the heart of West Los Angeles.The Principal Research and Development (R&D) Engineer oversees and participates in the capture, planning, design, prototyping, and verification of wireless technology projects.Technical management of R&D pro...
Assist counsel with regulatory and internal reviews, including, but not limited to, coordinating e-Discovery collections, executing and analyzing transactional reports, conducting legal research, coordinating document productions, and preparation of regulatory responses. Support regulatory change ma...