Overview
On Site
USD 50.00 - 68.00 per hour
Full Time
Skills
Regulatory affairs
Palo Alto
Regulatory Compliance
ISO 13485
Microsoft Word
Marketing
Documentation
Auditing
Training
FDA
Computer hardware
ISO 9000
Teamwork
Collaboration
Communication
Design
Microsoft Excel
Adobe
Job Details
Location: Palo Alto, CA
Salary: $50.00 USD Hourly - $68.00 USD Hourly
Description: Our client is currently seeking a Regulatory Affairs for a 12 month + contract.
Hybrid position, 2 days in office (Palo Alto, CA).
Position Description:
*Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices according to regulatory requirements
* Identifies, analyzes and implements country specific requirements necessary for product related submissions.
*Recommend strategies for earliest possible approvals for marketing applications
* Performs regulatory projects or acts as a member of the project steering group.
* Submits required documentation/information to local authorities or internal.
* Initiates and escalates necessary activities if deviations are identified.
* Ensures creation of adequate documentation for audits/inspections.
* Performs training within the organization in country specific regulatory requirements, if applicable. *Write and maintain submissions procedures, work instructions and templates relevant for maintaining regulatory compliance.
* Performs review of promotional material for regulatory compliance according to country specific requirements. Impacts: Is expected to adopt existing concepts, methodologies, etc. in order to create and open up new ways of approaching and fulfilling specific internal and external client requests or project requirements.
Experience: 5-8 years.
Product Registration Experience:
Experience with FDA 510(k) applications, Health Canada license applications and EU MDR technical files
Knowledge of regulatory guidance documents and requirements for product classification determination, FDA 510(k) submissions, Health Canada license Applications and EU MDR technical files.
Knowledge of regulatory guidance documents (FDA, Health Canada, EU MDR) for determining if a product change requires a regulatory submission (software and hardware devices).
Working knowledge of ISO 13485, IEC 62304, IEC 62366, ISO 14971, ISO 10993-1 as evidenced by coursework or submissions that required use of each standard
Teamwork and collaboration: Excellent communication and interpersonal skills to collaborate across departments and interact with design and development teams.
Experience with Business Tools: Proficient in utilizing business tools such as: E-mail, Microsoft Word, Excel, PowerPoint, and Adobe Pro.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!
Salary: $50.00 USD Hourly - $68.00 USD Hourly
Description: Our client is currently seeking a Regulatory Affairs for a 12 month + contract.
Hybrid position, 2 days in office (Palo Alto, CA).
Position Description:
*Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices according to regulatory requirements
* Identifies, analyzes and implements country specific requirements necessary for product related submissions.
*Recommend strategies for earliest possible approvals for marketing applications
* Performs regulatory projects or acts as a member of the project steering group.
* Submits required documentation/information to local authorities or internal.
* Initiates and escalates necessary activities if deviations are identified.
* Ensures creation of adequate documentation for audits/inspections.
* Performs training within the organization in country specific regulatory requirements, if applicable. *Write and maintain submissions procedures, work instructions and templates relevant for maintaining regulatory compliance.
* Performs review of promotional material for regulatory compliance according to country specific requirements. Impacts: Is expected to adopt existing concepts, methodologies, etc. in order to create and open up new ways of approaching and fulfilling specific internal and external client requests or project requirements.
Experience: 5-8 years.
Product Registration Experience:
Experience with FDA 510(k) applications, Health Canada license applications and EU MDR technical files
Knowledge of regulatory guidance documents and requirements for product classification determination, FDA 510(k) submissions, Health Canada license Applications and EU MDR technical files.
Knowledge of regulatory guidance documents (FDA, Health Canada, EU MDR) for determining if a product change requires a regulatory submission (software and hardware devices).
Working knowledge of ISO 13485, IEC 62304, IEC 62366, ISO 14971, ISO 10993-1 as evidenced by coursework or submissions that required use of each standard
Teamwork and collaboration: Excellent communication and interpersonal skills to collaborate across departments and interact with design and development teams.
Experience with Business Tools: Proficient in utilizing business tools such as: E-mail, Microsoft Word, Excel, PowerPoint, and Adobe Pro.
Contact:
This job and many more are available through The Judge Group. Please apply with us today!