Regulatory Affairs Professional
Regulatory Affairs Professional
Posted on :
20-01-2025
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1 Vacancy
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Job Description
Job Title: Regulatory Affairs Professional
Job Location: Bengaluru Karnataka India
Job Location Type: Onsite
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
Experience: 610 years
Qualifications:
You have successfully completed a course of studies in a technical or clinical field preferably in engineering medicine medical engineering or (medical) informatics
You can offer extensive professional experience in regulatory affairs for Software as Medical Device SaaS and/or cloud deployments
You have a sound knowledge of international laws standards and regulations for licensing medical devices and of the business processes of medical device manufacturers (e.g. MDD/MDR 21CFR 820; ISO 13485; IEC 62304; IEC 62366; ISO 14971)
Your profile also includes a knowledge of regulatory requirements for the clinical evaluation of software for medical devices
Experience in process or quality management would be an advantage
Your Attributes And Skills:
You also have team and communication skills initiative and a structured targetoriented way of working
You champion the success of Siemens Healthineers with drive and passion
Roles and Responsibilities:
Ensure the medical device products comply with the regulations of the regions where it is planned to be marketed and sold.
Maintaining a good understanding of new and existing regulations standards and guidances that may impact their organization’s products and processes.
Collect collate and evaluate product specific information in order to create and update the dossiers that must be submitted for new product licenses and license renewals.
Prepare submissions for regulatory registration and renewals
Maintaining data and files on country registrations for future reference particularly in the event of an audit by a regulatory agency
Preparing for and supporting internal regulatory and thirdparty audits as necessary
Collaborate with the project teams and explaining regulatory requirements procedures and policies to all employees and stakeholders as necessary.
Able to work in cross functional teams with good communication & interpersonal skills
Qualifications:
You have successfully completed a course of studies in a technical or clinical field preferably in engineering medicine medical engineering or (medical) informatics
You can offer extensive professional experience in regulatory affairs for Software as Medical Device SaaS and/or cloud deployments
You have a sound knowledge of international laws standards and regulations for licensing medical devices and of the business processes of medical device manufacturers (e.g. MDD/MDR 21CFR 820; ISO 13485; IEC 62304; IEC 62366; ISO 14971)
Your profile also includes a knowledge of regulatory requirements for the clinical evaluation of software for medical devices
Experience in process or quality management would be an advantage
Your Attributes And Skills:
- You are businessfluent in English enabling you to operate successfully in our international context; knowledge of German would be an advantage
You also have team and communication skills initiative and a structured targetoriented way of working
You champion the success of Siemens Healthineers with drive and passion
Roles and Responsibilities:
Ensure the medical device products comply with the regulations of the regions where it is planned to be marketed and sold.
Maintaining a good understanding of new and existing regulations standards and guidances that may impact their organization’s products and processes.
Collect collate and evaluate product specific information in order to create and update the dossiers that must be submitted for new product licenses and license renewals.
Prepare submissions for regulatory registration and renewals
Maintaining data and files on country registrations for future reference particularly in the event of an audit by a regulatory agency
Preparing for and supporting internal regulatory and thirdparty audits as necessary
Collaborate with the project teams and explaining regulatory requirements procedures and policies to all employees and stakeholders as necessary.
Able to work in cross functional teams with good communication & interpersonal skills
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Employment Type
Full Time
Key Skills
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