Regulatory Affairs Specialist - New Delhi - Bo International

+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 ...

We are seeking · a B.tech Biotechnology(Fresher) Regulatory and Clinical Affairs Specialist with expertise in regulatory compliance for medical devices across the EU, India, and the US. · ...

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

Key Responsibilities: · Prepare, review, and maintain software-related regulatory documentation for medical devices. · Ensure compliance with international regulatory standards including IEC standards, US FDA, EU MDR, and ISO 13485. · Support preparation and maintenance of Techni ...

Key Responsibilities: · Prepare, review, and maintain · software-related regulatory documentation · for medical devices. · Ensure compliance with international regulatory standards including · IEC standards, US FDA, EU MDR, and ISO 13485 · . · Support preparation and maintenance ...

Job Description · Primary purpose and function of this position: · To support RA associates in all administrative activities related to registration, electronic submission, maintenance of Drug Master Files (DMF) and answering customers requests. · Duties and Responsibilities: · P ...

We are looking for a highly skilled and experienced Quality & Regulatory Affairs Specialist to join our team at Naukri Healthcare Jobs, located in the Pharmaceutical and Life Sciences industry. The ideal candidate will have a strong background in quality control and regulatory af ...

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 ...

+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 ...

Document Coordination: Collaborate with Division contacts to obtain essential documents required by Taiwan RAQA during the registration process, including license and QSD applications. · Relationship Management: Establish and maintain a positive working relationship with Taiwan R ...

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

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. · ...

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. · ...

Looking for MBBS/MD/ DM/ BDS/ MDS with minimum 5 years of corporate experience in HO (Head Office) environment. · Demonstrating extensive knowledge of all clinical and scientific data for Medtronic products and maintaining a deep understanding of the science behind them. · Provi ...

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

Supporting the RA-FDF Team and contributing in the regulatory activities in order to achieve the objectives of the department which are:  obtaining global approval for CENTRIENT products, including the lifecycle management of the registration dossiers according to business planni ...

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

We seek a dedicated and detail-oriented Regulatory Assistant and Project Management Specialist. · ...