Regulatory Affairs - Noida

The Manager - Regulatory Affairs will be responsible for overseeing US regulatory operations, · 12-15 years of experience in US Regulatory AffairsProven expertise in USFDA regulatory strategy and submissions ...

The Regulatory Specialist will support MIBG I-131 clinical programs and other JDI innovative products in the pipeline. · ...

The Manager - Regulatory Affairs will be responsible for overseeing US regulatory operations and ensuring compliance for product portfolios in the US market. · ...

The Manager - Regulatory Affairs will be responsible for overseeing US regulatory operations. · ...

The employee will develop and maintain strong client relationships, participate in regulatory processes to gain marketing authorizations for human and veterinary medicinal products, prepare CMC documents, · communicate with clients and Health Authorities, · and responsible for pl ...

The Regulatory Specialist will support MIBG I-131 clinical programs and other JDI innovative products in the pipeline. · Challenges: · SCOPE and SIZE OF THE ROLE (Please indicate key metrics defining the size and scope of the role) · ...

We are looking for a Regulatory Affairs trainee to participate in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products. · ...

To support MIBG I-131 clinical programs and other JDI innovative products in the pipeline, The Regulatory Specialist will be reporting to the director of Regulatory Affairs and support the development of regulatory strategies related to JDI clinical programs, marketing applicatio ...

Manage regulatory compliance for domestic and international regulations like EU REACH, DMF filing, life cycle management of active ingredients/supplements category. · ...

+Participation in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products (applications renewals variations) including medical devices cosmetics food supplements and herbal products. · +University degree in Life Science · ...

+Job summary · We're Hiring Senior Executive – Food Regulatory Affairs (FSSEA Licensing) · +ResponsibilitiesManage key regulatory compliance activities with a strong focus on FSSAI Licensing and FoSCoS operations. · ...

This role involves leading end-to-end statutory approvals for renewable energy projects. · ...

More than 4 years of experience in Wind industry. · Monitor, interpret, and ensure compliance with local, state, and national regulations related to wind energy development. · Lead or assist in obtaining necessary permits and licenses for wind farm construction and operation. · ...

Prepare regulatory documentation and coordinate with sales team to collect required documents. Liaise with factory department to ensure preparation of technical files and support documents. · ...

+Job summary · We are seeking a detail-oriented Regulatory Affairs Specialist to manage regulatory compliance across FSSAI, · AYUSH, · and Legal Metrology for nutraceutical and herbal products.+Ensure FSSAI compliance by reviewing formulations, · Manage new product endorsements · ...

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 seeking a detail-oriented · Drug Regulatory Affairs Specialist to join our dynamic team. In this role, you will play a crucial part in ensuring compliance with regulatory requirements for our products while collaborating closely with cross-functional teams to drive succes ...

The Regulatory Affairs Executive will be responsible for preparing and reviewing regulatory documentation ensuring compliance with regulatory requirements developing and managing regulatory strategies and supporting the company s efforts to meet international standards. · ...

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 ...