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Please contact Abdul on "" OR email me at ""
*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 Siemens/Varian 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.
Experience: 5-8 years.
Knowledge: Deep professional know-how and experience in one Sub Job Family. Masters domain. Transfers and applies know-how to / in various contexts. Solid professional judgment and problem solving competence. Improves existing processes and approaches
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.
Please contact Abdul on "" OR email me at ""
Full Time
IT Outsourcing & Consulting
$112k-142k (estimate)
05/18/2024
07/17/2024
apninc.com
NEWARK, CA
25 - 50
1996
Private
ASLAM CHANDIWALLI
$10M - $50M
IT Outsourcing & Consulting
The job skills required for Sr. Regulatory Affairs Specialist include ISO, Regulatory Compliance, Product Registration, Problem Solving, Collaboration, PowerPoint, etc. Having related job skills and expertise will give you an advantage when applying to be a Sr. Regulatory Affairs Specialist. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Sr. Regulatory Affairs Specialist. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Sr. Regulatory Affairs Specialist positions, which can be used as a reference in future career path planning. As a Sr. Regulatory Affairs Specialist, it can be promoted into senior positions as a Regulatory Affairs Specialist IV that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Sr. Regulatory Affairs Specialist. You can explore the career advancement for a Sr. Regulatory Affairs Specialist below and select your interested title to get hiring information.