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...
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...
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 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...
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...
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. ...
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 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...
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: 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. ...
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...
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...
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...
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 stakeholders such as Project managers, Manu...
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...
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, ...
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...
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...
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: 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...
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. ...
For further inquiries regarding the following opportunity, please contact one of our Talent Specialists<br /> Rashi at 630 847 1027<br /> Divya at 224 369 2969</b></div> <div> </div> <div><b>Title: Specialist Regulatory Affairs, EURI/ MENAP<br />...
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...