Regulatory Affairs Consultant (Navi Mumbai)

Regulatory Affairs Consultant (Navi Mumbai)

Position – Regulatory Consultant
Company Information
We are a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. We have our head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. We have been providing high quality & timely consulting service to the Pharmaceutical Industry in India and internationally. We have a young and committed team of GMP and Regulatory Experts. We are inviting applications for the role of Regulatory Consultant and are looking for agile, driven individuals with strong initiative who can thrive in the entrepreneurial environment at our firm.
Role & Responsibilities
The person will be responsible for Regulatory consulting services at the firm. The responsibilities of this position include, but are not limited to, the following:
Ownership for assigned regulatory projects including dossier writing, submissions, approval tracking, query resolution across Developed markets (EU, US,



UK & Australia) and Emerging markets
Ensure regulatory compliance, accuracy, timely completion, version control & adherence to internal SOPs
Providing strategic input to the Management and Partners on regulatory projects
Keep abreast of new developments in regulations across all critical health authorities
Experience & Qualifications
Regulatory affairs experience in small molecules for a minimum of 6-10 years is mandatory
Must be well versed with ICH CTD guidelines and other regulatory guidelines from developed markets (US, EU, Australia/ UK).
Must have hands-on experience in regulatory submissions pertaining to generics/ small molecules in US/ EU/Australia/ UK
Basic Computer knowledge
Strong & Flawless communication skills.
Accuracy and attention to detail.

📌 Regulatory Affairs Consultant (Navi Mumbai)
🏢 Metina PharmConsulting
📍 Navi Mumbai