July 2025

Responsible for the ordering and tracking of specific regulatory requirements such as registration samples, Certificates of Pharmaceutical Product, Legal documentation e.g. Letters of Authorisation, Powers of Attorney, Translations of regulatory documentation

Candidate will be responsible for preparing and managing regulatory dossiers, coordinating with regulatory authorities for EU and ASEAN markets and providing guidance on regulatory requirements to internal teams

Make sure the relevant documents for various product families are available to support risk management, change control processes and design integrity.

Perform analysis of raw materials and finished products using UV, IR, HPLC, UPLC, GC, LCMS, etc. Ensure adherence to SOPs, GMP, and ALCOA principles during shift operations.

Accurately translate understanding of regulatory requirements and corporate policies governing documents for regulatory submission into execution of timely and compliant analyses and presentations of safety data and benefit-risk assessment in documents.

B.Pharm or Approved Diploma in Pharmacy from an institute recongnised by the Pharmacy council of India and registered as Pharmacist under the Pharmacy Act 1948

Masters in Natural or Pharmaceutical Sciences/ MVSc/ Animal Sciences OR degree in Engineering or Technology or Medicine from a recognized University or equivalent

Should have completed D.Pharm or B.Pharm Coures from any recognized educational institution. Should have registered with State Pharmacy Council. Primary Health Centre

M.Pharm / MS Pharm / M.Tech. / M.Sc. with specialization in Medical Devices/ Biomedical Sciences/ Chemistry / Electronics / Biotechnology / Material Sciences / Nanoscience / Nanotechnology or equivalent.