Government Affairs Specialist - Delhi

+Job summary · We are hiring for an exciting opportunity with our esteemed client, a global leader in diagnostic and medical technology. · ++Responsibilities · ...

We are hiring for an exciting opportunity with our esteemed client,a global leader in diagnostic and medical technology, · Prepare & submit regulatory dossiers for CDSCO (Import & Manufacturing Licenses) · , · , · , ...

We're hiring an exciting opportunity with our esteemed client in diagnostic and medical technology. · Prepare & submit regulatory dossiers for CDSCO (Import & Manufacturing Licenses) · Hands-on submissions via CDSCO SUGAM & NSWS portals · Maintain regulatory documentation, tracke ...

· At Beckman Coulter Diagnostics, you'll join a team where you can be heard, · be supported, · and always be yourself. · We're building a culture that celebrates backgrounds,experiences, and perspectives of all our associates. · The Principal Specialist defines and executes regu ...

This job is with Danaher an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. · ...

The Senior Specialist, Regulatory Affairs will be responsible for Pre-evaluation of Reference Country Strategies, Deviation creation, Pre-evaluation of DLs, CCDS Update process till Global Dispatch, Binder creation etc. Participate in regulatory processes to gain and maintain mar ...

We are looking for a highly skilled and experienced Regulatory Affairs Specialist to join our team in the Pharma Company. · Develop and implement regulatory strategies for medical device approvals. · Prepare and review regulatory submissions, including clinical trial applications ...

The Regulatory Affairs Specialist will have an exciting opportunity to work with the Commercial Regulatory Affairs Team and help business with product registration in India Sub Continent. · ...

Regulatory Affairs Specialist Job Description · This role involves supporting remediation activities including developing strategies for literature reviews and evaluating data from various sources. · ...

We are looking for Regulatory Affairs Specialist responsible for regulatory submissions product registrations license renewals and compliance for medical devices in India and other countries. · Ensure regulatory compliance with relevant global medical device regulations. · Prepar ...

+Total Exp - 5-8 years · Supports on CER remediation including developing search strategy for literature review and state-of-the-art (SotA); evaluating the data from MAUDE, HPRA or MHRA compiling information from various sources. · Prepare/ update Clinical Evaluation Reports (CER ...

TCI Group is seeking an experienced Government Affairs Specialist to provide strategic leadership on government policy regulatory compliance and stakeholder engagement impacting logistics supply chain operations. · ...

+ At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. · ...

We are seeking an experienced Government Affairs Specialist to provide strategic leadership on government policy and regulatory compliance impacting logistics and supply chain operations. · ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. · ...

This role supports the RA-FDF Team in regulatory activities to achieve departmental objectives including global approval for CENTRIENT products. · ...

Support the RA-FDF team and contribute to regulatory activities to achieve department objectives including global approval for CENTRIENT products and lifecycle management of registration dossiers according to business planning. · ...

The Regulatory Affairs Specialist will support the RA-FDF team and contribute to regulatory activities to achieve departmental objectives. · ...

The company is hiring for the position of Regulatory Affairs Specialist Medical Devices with total experience of 5-8 years. · ...

We are looking for the Primary scientific face of the organization to 'Thought Leaders' & physicians for a given therapy area. · MBBS with full time post-graduate qualification of at least 2-years' duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institu ...