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. · ...

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 ...

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 ...

+Preparation and submission of registration dossier and renewal application for ANDA / ROW submission. · +preparation and submission of registration dossier, renewal application and variation application for ANDA / ROW submissionPreparation of respective CTD sections and submissi ...

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 ...

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. · ...

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

NuVvaGen Bioscience (P) Ltd, an export-focused manufacturing company, seeks a Regulatory Affairs Manager. Key responsibilities include: · Preparation and filing of new drug applications with regulatory authorities. · Liaising with CDSCO, State FDA, DCGI, and port offices for vari ...

Job Title: Head of Regulatory Affairs · The ideal candidate will possess deep domain expertise in regulatory requirements across international markets, especially in the generics pharmaceutical space. · We are seeking an accomplished Regulatory Affairs leader with over 20 years o ...

regulatory affairs manager api dmf experience:6+ years review evaluate api drug master files for regulatory compliance assess manufacturing processes controls specifications analytical data ensure compliance global regulatory guidelines us fda eu who ich support regulatory submis ...

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

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. · ...

Support regulatory affairs activities related to APIs and pharmaceutical intermediates. · ...

We are seeking an experienced Regulatory Affairs professional to manage global regulatory submissions and lifecycle activities across Africa, LATAM, Asia, · and other assigned markets.Review batch manufacturing records. · Serve as Product Lead for assigned products. · ...

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