IntePros
Overview
IntePros is currently looking for a
Sr. Regulatory Affairs Specialist
to join one of our growing Medical Device clients in Audubon, PA. The
Sr. Regulatory Affairs Specialist
will coordinate and prepare document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking and control systems. Keeps abreast of regulatory procedures and changes. Recommends strategies for earliest possible approvals of clinical trials applications.
Responsibilities
Determines the appropriate regulatory strategy for new products and documents all related activities to remain in compliance
Demonstrates global regulatory expertise in product submissions and evaluates changes with local regulations
Collaborates with various departments to review the required plans, procedures and regulatory decisions for new or existing products
Reviews regulatory requirements from other departments for new product designs or changes to existing designs
Reviews technical publications, articles, and abstracts to stay abreast of regulatory and technical developments in the industry
Prepares and maintains regulatory pre-market submissions and other pre-market filings to assist in acquiring appropriate commercial distribution clearances
Supports product import by providing applicable regulatory documentation and certificates
Qualifications
Typically requires a minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree; or a PhD without experience; or equivalent work experience
5+ years of related experience in the medical device industry
Understanding of regulatory requirements throughout the product lifecycle
Solid understanding of regulatory terminology, pre-market submission types, and requirements
Able to evaluate regulatory impact of proposed product and process changes
Capable multi-tasking skills with the ability to project plan and meet deadlines
Result driven with a sense of responsibility, urgency and ability to perform under pressure
#J-18808-Ljbffr
IntePros is currently looking for a
Sr. Regulatory Affairs Specialist
to join one of our growing Medical Device clients in Audubon, PA. The
Sr. Regulatory Affairs Specialist
will coordinate and prepare document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking and control systems. Keeps abreast of regulatory procedures and changes. Recommends strategies for earliest possible approvals of clinical trials applications.
Responsibilities
Determines the appropriate regulatory strategy for new products and documents all related activities to remain in compliance
Demonstrates global regulatory expertise in product submissions and evaluates changes with local regulations
Collaborates with various departments to review the required plans, procedures and regulatory decisions for new or existing products
Reviews regulatory requirements from other departments for new product designs or changes to existing designs
Reviews technical publications, articles, and abstracts to stay abreast of regulatory and technical developments in the industry
Prepares and maintains regulatory pre-market submissions and other pre-market filings to assist in acquiring appropriate commercial distribution clearances
Supports product import by providing applicable regulatory documentation and certificates
Qualifications
Typically requires a minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree; or a PhD without experience; or equivalent work experience
5+ years of related experience in the medical device industry
Understanding of regulatory requirements throughout the product lifecycle
Solid understanding of regulatory terminology, pre-market submission types, and requirements
Able to evaluate regulatory impact of proposed product and process changes
Capable multi-tasking skills with the ability to project plan and meet deadlines
Result driven with a sense of responsibility, urgency and ability to perform under pressure
#J-18808-Ljbffr