Lead Consultant – Regulatory Affairs - Mumbai, Maharashtra

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai (GRASC – Team). The person will be reporting to the Manager Regulatory Affairs. · Author Safety Data Sheets for multiple geographies across the globe as per applicable hazard commu ...

The Regulatory Affairs Manager will oversee all functions of the department including scheduling activities, dossier preparation and review, regulatory submissions and approvals, task management and timeliness, compliance assurance, team leadership and development. · ...

Develop and implement regulatory strategies to ensure compliance with EU regulations. · Collaborate with cross-functional teams to prepare and submit regulatory documents. · Conduct thorough reviews of regulatory submissions to ensure accuracy and completeness. · Build and mainta ...

Candidates should have 5 -13 years of experience in pharmaceutical regulatory affairs . · ...

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai.The GRASC – Team is an integral part of the Diversey regulatory function. · Handle key regulatory activities like compliance workflows, creation of SDS, labels, product registratio ...

We are seeking an experienced Regulatory Affairs Specialist to join our team at Associate Allied Chemicals (India) Pvt. Ltd. · Prepare, review, and maintain regulatory documents such as SDSs · , Assist in compiling dossiers for product registration across various regions · , Liai ...

preparation and submission of registration dossier, renewal application and variation application for ANDA / ROW submission · Preparation of respective CTD sections and submission of final query response to agency · Preparation and submission of documents for national phase to re ...

Develop and implement regulatory strategies for API products. · Prepare and review regulatory submissions, including applications and reports. · Collaborate with cross-functional teams to ensure compliance with regulatory requirements. · Conduct thorough reviews of regulatory doc ...

Coordination with internal and external parties for regulatory filing related documentation. · ...

Manage domestic regulatory submissions for pharmaceutical finished formulations in compliance with Indian regulatory requirements Compile review and maintain ACTD/CTD dossiers as per CDSCO and other applicable local regulations Handle online regulatory submissions through Sugam p ...

Regulatory Affairs role involves coordination with internal and external parties for regulatory filing related documentation. · ...

We have an urgent opening coming up with one of the leading Pharmaceutical organization Mumbai (Kandivali West) for the role of Regulatory Affairs. · Should be well versed with Regulatory Affairs Guidelines of South East Asia Africa Middle East LATAM ROW. · Knowledge of Preparati ...

Concept Pharma is looking for a qualified and experienced Regulatory Affairs professional to manage regulatory submissions and ensure compliance with applicable regulations for pharmaceutical products in domestic and international markets. · ...

We are looking for a highly skilled and experienced Regulatory Affairs Officer to join our team at a reputed Pharma Company. · Bachelor's degree in Life Sciences or a related field. · Minimum 5 years of experience in regulatory affairs within the pharma industry. · ...

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai. · ...

We are looking for an experienced Regulatory Affairs to manage and oversee regulatory submissions and compliance for Emerging or ROW (Rest of the World) markets. · ...

Manager Regulatory Affairs (EU/UK): Handle EU & UK MA filings, eCTD submissions, lifecycle management & variations. · 14+ yrs pharma regulatory exp. · ...

We are looking for a highly skilled and experienced Regulatory Affairs professional to join our team at a reputed Pharma Company. · ...

We are looking for a highly skilled and experienced Regulatory Affairs Specialist to join our team at a reputed Pharma Company. · ...

We are recruiting an Executive Regulatory Affairs to contribute regulatory expertise in various aspects including regulatory submissions, right first-time dossiers, timely addressal of queries etc. for various product categories such as Cosmetics Commodities etc. · ...

The Regulatory Affairs Manager will provide support to the Regulatory Affairs Manager and assist in independent preparation of CTD dossier along with complete regulatory compilation like Notarized / Apostle documents registration samples etc for timely registration of the product ...