Job Description
About Qure.ai:
Qure.ai develops artificial intelligence enabled products and platforms for healthcare diagnostics. We have a talented team of data scientists, deep learning engineers, regulatory experts, commercial team and client managers. Founded in 2016, we apply the latest AI research to healthcare problems and develop innovative solutions that are revolutionizing the way patients are diagnosed and treated. Our solutions have impacted more than 4 million lives in 50 countries.
Qure is an equal opportunity employer. Artificial Intelligence technology evolves fast, and healthcare regulators are striving to keep up.
Job Description
As Regulatory Affairs Specialist , you will develop and execute strategies to bring this newly developed class of medical devices to market.
Your
Responsibilities
Set industry-leading standards and benchmarks for regulatory excellence in healthcare AI software documentation
Help regulators understand healthcare AI software development processes
Develop and communicate a solid understanding of the Risks and benefits of medical imaging AI
Set up, maintain and document quality management systems suited to the recently developed EU and US regulatory requirements
Manage internal and external audits
Keep up with rapidly evolving global market regulation on AI in medical imaging
Liaise closely with clinical and R&D teams to ensure that products are cleared fast as they are developed
Your Skills,
Qualifications , and Personal attributes
Demonstrated history of driving products from development through to regulatory approval (CE and US FDA)
Experience with software devices or AI software
Work experience of 2-7 years
Familiarity with IEC 62304 and ISO 14+71
Exposure to MDR process for software devices
Experience with FDA technical documentation
Demonstrated ability to work with regulatory authorities to develop new regulatory processes in areas with few precedents or standards
Technical undergraduate degree, advanced degree preferred
You will be part of a rapidly growing organization, with an opportunity to work alongside the best minds in the industry. Competitive compensation and rewards, opportunity to grow with a young company.
Location:
Mumbai
Inclusive workspace:
(Use the "Apply for this Job" box below).-10
By submitting your information and application, you confirm that you have read and agree to the Applicant Privacy Policy
Qure.ai develops artificial intelligence enabled products and platforms for healthcare diagnostics. We have a talented team of data scientists, deep learning engineers, regulatory experts, commercial team and client managers. Founded in 2016, we apply the latest AI research to healthcare problems and develop innovative solutions that are revolutionizing the way patients are diagnosed and treated. Our solutions have impacted more than 4 million lives in 50 countries.
Qure is an equal opportunity employer. Artificial Intelligence technology evolves fast, and healthcare regulators are striving to keep up.
Job Description
As Regulatory Affairs Specialist , you will develop and execute strategies to bring this newly developed class of medical devices to market.
Your
Responsibilities
Set industry-leading standards and benchmarks for regulatory excellence in healthcare AI software documentation
Help regulators understand healthcare AI software development processes
Develop and communicate a solid understanding of the Risks and benefits of medical imaging AI
Set up, maintain and document quality management systems suited to the recently developed EU and US regulatory requirements
Manage internal and external audits
Keep up with rapidly evolving global market regulation on AI in medical imaging
Liaise closely with clinical and R&D teams to ensure that products are cleared fast as they are developed
Your Skills,
Qualifications , and Personal attributes
Demonstrated history of driving products from development through to regulatory approval (CE and US FDA)
Experience with software devices or AI software
Work experience of 2-7 years
Familiarity with IEC 62304 and ISO 14+71
Exposure to MDR process for software devices
Experience with FDA technical documentation
Demonstrated ability to work with regulatory authorities to develop new regulatory processes in areas with few precedents or standards
Technical undergraduate degree, advanced degree preferred
You will be part of a rapidly growing organization, with an opportunity to work alongside the best minds in the industry. Competitive compensation and rewards, opportunity to grow with a young company.
Location:
Mumbai
Inclusive workspace:
(Use the "Apply for this Job" box below).-10
By submitting your information and application, you confirm that you have read and agree to the Applicant Privacy Policy
💡 Quick Summary
Seeking a career-building opportunity? The Regulatory Affairs Specialist position is now open for candidates interested in the Software Developer Jobs sector. This role in Mumbai offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Software Developer Jobs is a plus.