Regulatory Affairs - Irvine

Planifica, coordina e implementa la presentación de solicitudes regulatorias para productos que requieren aprobación del gobierno. · ...

The Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function and is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) experience ...

The Regulatory Affairs Specialist will ensure BaRupOn's pharmacy manufacturing and healthcare operations meet all applicable regulatory requirements. · ...

The position requires a Regulatory Affairs Specialist to plan and implement regulatory submissions for medical devices. The ideal candidate should have mid-level experience and knowledge of healthcare-related regulations. · ...

The Regulatory Affairs Specialist will provide support to the Director of Regulatory Affairs in relation to the Company's regulatory compliance efforts. · ...

· We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting 510(k) notifications. · Leads the preparation, submission, and negotiation of 510(k) premarket notification ...

The Regulatory Affairs Specialist is responsible for planning coordinating and implementing regulatory Submissions for products that require government approval. · ...

The Regulatory Affairs Specialist will provide support to the Director of Regulatory Affairs in relation to the Company's regulatory compliance efforts. · Assist in managing regulatory affairs matters for the company · Responsible for supporting registration/regulatory needs to m ...

Regulatory Affairs is responsible for planning coordinating and implementing regulatory Submissions for products that require government approval. · ...

+ A large medical device company · is looking for a Regulatory Affairs Coordinator · to help with compliance activities.1+ years of experience in regulatory affairs · Strong experience in the life sciences industry · Bachelor's degree · ...

The Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function.The position is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) e ...

The Regulatory Affairs Specialist will provide support to the Director of Regulatory Affairs in relation to the Company's regulatory compliance efforts. · Assist in managing regulatory affairs matters for the company · ...

A large medical device company is looking for a Regulatory Affairs Coordinator to help with compliance activities. The responsibilities include but are not limited to: Prepares, dispatches and files routine Regulatory Affairs documentation Collaborates with Regulatory Affairs sta ...

We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting · 510(k) notifications. This individual will lead regulatory strategy and submissions for · devices requiring ...

This role will focus on supporting the EU's In Vitro Diagnostic Regulation (IVDR) transition activities impacting all products currently CE Marked under the IVD Directive. · ...

+10 months duration. Three days a week in Irvine, California. Responsible for planning regulatory submissions for products requiring government approval. · Apply relevant regulations to further product submissions of basic to medium complexity. · Contribute to strategic direction ...

This job involves planning coordinating and implementing regulatory submissions for products requiring government approval. · Demonstrates working knowledge of healthcare-related regulations. · Demonstrates in-depth knowledge of preparing a submission. · ...

Responsible for planning, coordinating and implementing regulatory Submissions for products that require government approval. · ...

+Job summary · Regulatory Affairs is responsible for planning coordinating and implementing regulatory Submissions for products that require government approval. · +Demonstrates working knowledge of healthcare-related regulations · Demonstrates in-depth knowledge of preparing a s ...

Job Title: · Regulatory Affairs Specialist II · Join our client's Regulatory Affairs team to support the transition to the EU's In Vitro Diagnostic Regulation (IVDR), impacting all CE-marked IVD products. · ...