Regulatory Affairs Specialist to work on Cybersecurity related regulations. The individual will also collaborate with regulatory affairs to develop, implement, and maintain software and cybersecurity framework and procedures to maintain and ensure compliance with medical device regulatory requiremen...
The Regulatory Specialist will support the Regulatory Department with implementing and maintaining processes and procedures intended to ensure Reynolds' products are compliant with all applicable laws, regulations, and internal policies. Regulatory Specialist (Temporary). Assist the Senior Regulator...
Regulatory Affairs Ops Specialist. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Company’s products. Compile and submit, in a time...
Regulatory Affairs Ops Specialist I. Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types. Creating timelines for regulatory filings. Overseeing authoring and reviewing of regulatory documents. ...
Our client is looking for a Regulatory Specialist to review raw materials. Assist the Senior Regulatory Counsel and Senior Regulatory Manager with developing strategies and implementing systems designed to ensure compliance with applicable laws and regulations. Engage with regulatory agencies and in...
Job Title: Specialist Regulatory Affairs. Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes. Direct interaction with RA functions including Regulatory Operations, Submissions Execution, Regulatory Project Management, Strategic Area and other s...
Regulatory Affairs Specialist II. Provides regulatory support to regional regulatory teams to assist with submissions, license renewals, and license amendments. Provides regulatory support for diagnostic product development and commercial diagnostic products. Develops regulatory strategies for produ...
Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes. Support Regulatory submissions for Food, FSMP, Enteral Nutrition, IF & FUF, Drug for EURI/ MENAP/ global. Partnership with affiliates to support regulatory agency interactions to expedite appr...
Title: Specialist Regulatory Affairs, EURI/ MENAP. Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes. Direct interaction with RA functions including Regulatory Operations, Submissions Execution, Regulatory Project Management, Strategic Area an...
Regulatory Affairs Ops Specialist. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Company’s products. Compile and submit, in a time...
Title: Regulatory Affairs Ops Specialist II. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Client's products. Compile and submit, ...
Under supervision responsible for implementing global regulatory strategies, acquiring and maintaining marketing authorizations for product(s) and communicating general regulatory requirements in support of licensing Baxter’s products. With direction, develop and implement regulatory project plans. ...
GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Regulatory Briefing Documents, ICH Regulations. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of gener...
Title: Specialist Regulatory Affairs, EURI/ MENAP. Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes. Direct interaction with RA functions including Regulatory Operations, Submissions Execution, Regulatory Project Management, Strategic Area an...
Title: Specialist Regulatory Affairs, EURI/ MENAP. Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes. Direct interaction with RA functions including Regulatory Operations, Submissions Execution, Regulatory Project Management, Strategic Area an...
The Regulatory Specialist will support the Regulatory Department with implementing and maintaining processes and procedures intended to ensure Reynolds' products are compliant with all applicable laws, regulations, and internal policies. Regulatory Specialist (Temporary). Assist the Senior Regulator...
Represent international RA and demonstrate leadership in complex product development strategies by identifying and interpreting relevant regulatory requirements, and providing actionable regulatory guidance throughout the product development cycle prior to regulatory submission. Review protocols and...
Title: Regulatory Affairs Ops Specialist I. Managing the preparation of regulatory submissions for IND, ANDA, NDA, K, Clientrom, and other electronic submission types. Creating timelines for regulatory filings. Overseeing authoring and reviewing of regulatory documents. ...
Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types Creating timelines for regulatory filings Providing and maintain templates for authoring. Overseeing authoring and reviewing of regulatory documents QC submission documents. Ide...
Regulatory Affairs Specialist to work on Cybersecurity related regulations. The individual will also collaborate with regulatory affairs to develop, implement, and maintain software and cybersecurity framework and procedures to maintain and ensure compliance with medical device regulatory requiremen...
Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Acts as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments as needed. Reviews an...
The Regulatory Specialist will support the Regulatory Department with implementing and maintaining processes and procedures intended to ensure Reynolds’ products are compliant with all applicable laws, regulations, and internal policies. Regulatory Specialist (Temporary) . Assist the Senior Regulato...
Title: Regulatory Affairs Ops Specialist II. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Client’s products. Compile and submit, ...
Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Baxter’s products. Compile and submit, in a timely manner, regulatory documents acco...
Joule has a contract opening for a Regulatory Affairs Ops Specialist II that will be responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of...