Senior Executive 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 (GRASC – Team). · The Global Regulatory Affairs Service Center Team (GRASC – Team) is a chemical regulatory group at "Diversey – A Solenis company". The GRASC - Team is an integral ...

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 ...

Regulatory Affairs role involves 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 ...

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

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 ...

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 ...

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

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

Manage the regulatory process for Pharmaceutical Finished Formulations across CIS, LATAM, and Africa. · Compile and review ACTD and CTD dossiers to ensure accuracy and compliance. · Address and respond to any Ministry of Health (MOH) queries for dossiers submitted in relevant ter ...

We are looking for a highly skilled and experienced Officer Regulatory Affairs to join our team in the Pharmaceutical and Life Sciences industry. The ideal candidate will have a strong background in regulatory affairs and a passion for driving business growth. · Roles and Respons ...

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

To manage and execute regulatory strategies, submissions, approvals, · and lifecycle management activities for pharmaceutical products across ROW markets. · ...

Olive PharmaScience Ltd is a leading name in global healthcare innovation delivering high-quality pharmaceutical solutions for over 50 years. · Dossier preparation & submissions · Responses to queries / deficiencies · Product registrations & lifecycle management · ...

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. · ...