Regulatory affairs

9 May 2024

Hiring Experienced M.Pharm Candidates for Regulatory Affairs department at Natco Pharma

Hands on experience in compiling and review of the dossiers for ASEAN Markets, AFRICAN Region, Middle East and GCC Region, LATAM Region including Brazil and Mexico. Well versed with CTD and ACTD dossier compilation and registration requirements.

9 May 2024

Work as Regulatory Specialist MSR Coordination at GSK India

With minimal input from manager, manages multiple project assignments supporting Variations, Product Expansion dossiers, Renewals and regional projects simultaneously; MSR packages/documents will range in complexity

9 May 2024

Regulatory Affairs Specialist Require at Medicines Patent Pool

Autonomous with strong self-motivation and ability to work independently as well as in a highly collaborative and multicultural environment within short timelines.

9 May 2024

Johnson & Johnson Hiring Executive Packaging & Regulatory Affairs

Preparation of additional information or responses as requested by regulatory agencies. Prepare or maintain technical files as necessary to obtain and sustain product approval. Direct the collection and preparation of laboratory samples as requested by regulatory agencies.

7 May 2024

Require Regulatory Professional at Novo Nordisk

Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk.

6 May 2024

Opportunity for M.Pharm to Join Indian Pharmacopoeia Commission as Complaint Executive

Indian Pharmacopoeia Commission (IPC) is an Autonomous Institution of the Ministry of Health and Family Welfare, Govt. of India. IPC is created to set standards of drugs in the country. Its basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region. It publishes official documents for improving Quality of Medicines by way of adding new and updating existing monographs in the form of Indian Pharmacopoeia (IP).

4 May 2024

Regulatory Affairs Specialist Require at Medtronic

Prepare, review, file, and support premarket documents for global registrations for assigned projects. Collaborate with business unit and international regulatory affairs personnel to support marketing authorizations for assigned projects.

3 May 2024

Sanofi looking for Regulatory Affairs Manager

The Regulatory Manager is a scientific leadership role that leads the regulatory activities involved in the India, Srilanka, Nepal, Maldives market. The role provides the regulatory strategies, and regulatory submissions of new products for various brands in Rx, OTC, Food supplements in support of the new and existing portfolio

3 May 2024

Enzene Bioscience's Walk-in Drive for M.Pharm, MSc, MTech in Multiple Department

Mammalian and Microbial (Upstream Process): Media preparation, Filtration, Aseptic technique, Inoculum Handling, Handling of SU bioreactor/RM, Perfusion technology, upstream analytical instruments. Handling of SS Fermenter, Continuous centrifuge

3 May 2024

ADVANZ PHARMA looking for Regulatory Affairs Executive

Assessing Change request assigned to ensure regulatory assessment along with strategy and documents required for any regulatory submissions are shared with stakeholder in a timely fashion.

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Hiring Experienced M.Pharm Candidates for Regulatory Affairs department at Natco Pharma

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