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Regulatory Specialist
Des Plaines, IL
Job Description
OVERVIEW
We are currently searching for a skilled professional to join a well-known client's team as a Regulatory Specialist in Des Plaines, IL. The Regulatory Specialist role will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.
RESPONSIBILITIES
* Responsible for implementing and maintaining the effectiveness of the quality system.
* Supports manufacturing/operations day to day activities for change control.
* Provides consultation/advice to regulatory specialist for change control and product development.
* Provides regulatory direction/interpretation on team activities.
* Interprets and applies regulatory understanding to support of products and teams.
* Prepares U.S. regulatory submissions and/or registration documents for international affiliates and government agencies worldwide.
* Handles regulatory activities involved in documentation, labeling, field support.
* Applies regulatory and technical knowledge to a wide variety of complex work assignments.
* Maintains and ensures compliance to the appropriate quality system for the specific medical device(s) designed or manufactured that the individual supports.
* Ensures compliance to and is able to demonstrate knowledge of site and division level policies and procedures.
EXPERIENCE
Must have 1-2 years of experiences in Medical Device Reg Affairs
EDUCATION
BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.
To be a best-fit your strengths must include:
* Knowledge of regulations and standards affecting IVDs and/or biologics
* Have working knowledge in EU MDR
* Have working knowledge in Regulatory Change Assessments
* Have working knowledge in US and EU medical device submissions
* Work cross-functionally and in a matrixed environment
* Have experience with continuous improvement activities
509228
About Advanced Clinical
Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Our mission is to deliver a truly better clinical experience for our clients and candidates. To learn more about Advanced Clinical which has been named to Chicago Tribune's Top Workplaces, Chicago's Best and Brightest Companies, and Best of Staffing Talent & Client, visit http://www.advancedclinical.com.
Regarding your application
Please know that every completed application is carefully reviewed by the Advanced Clinical recruitment team. We understand the time commitment that is needed to prepare an application, so we respect your effort by thoughtfully reviewing and responding to each application. In return, we ask for your patience as careful review takes time, and we may not be able to respond to every application immediately.
We are currently searching for a skilled professional to join a well-known client's team as a Regulatory Specialist in Des Plaines, IL. The Regulatory Specialist role will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.
RESPONSIBILITIES
* Responsible for implementing and maintaining the effectiveness of the quality system.
* Supports manufacturing/operations day to day activities for change control.
* Provides consultation/advice to regulatory specialist for change control and product development.
* Provides regulatory direction/interpretation on team activities.
* Interprets and applies regulatory understanding to support of products and teams.
* Prepares U.S. regulatory submissions and/or registration documents for international affiliates and government agencies worldwide.
* Handles regulatory activities involved in documentation, labeling, field support.
* Applies regulatory and technical knowledge to a wide variety of complex work assignments.
* Maintains and ensures compliance to the appropriate quality system for the specific medical device(s) designed or manufactured that the individual supports.
* Ensures compliance to and is able to demonstrate knowledge of site and division level policies and procedures.
EXPERIENCE
Must have 1-2 years of experiences in Medical Device Reg Affairs
EDUCATION
BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical technology, etc.
To be a best-fit your strengths must include:
* Knowledge of regulations and standards affecting IVDs and/or biologics
* Have working knowledge in EU MDR
* Have working knowledge in Regulatory Change Assessments
* Have working knowledge in US and EU medical device submissions
* Work cross-functionally and in a matrixed environment
* Have experience with continuous improvement activities
509228
About Advanced Clinical
Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Our mission is to deliver a truly better clinical experience for our clients and candidates. To learn more about Advanced Clinical which has been named to Chicago Tribune's Top Workplaces, Chicago's Best and Brightest Companies, and Best of Staffing Talent & Client, visit http://www.advancedclinical.com.
Regarding your application
Please know that every completed application is carefully reviewed by the Advanced Clinical recruitment team. We understand the time commitment that is needed to prepare an application, so we respect your effort by thoughtfully reviewing and responding to each application. In return, we ask for your patience as careful review takes time, and we may not be able to respond to every application immediately.
Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Experience
1 to 2 years
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