Regulatory Affairs Manager, India

Ziqsy Ltd; India; On-site; INR 1,800,000 - 3,000,000; Full time

Job summary

Ziqsy Ltd. is seeking a Regulatory Affairs Manager for India to own the regulatory workstream for health, pharma or consumer products. You will map requirements, prepare registrations and maintain compliance evidence for launches and ongoing operations.

The role involves coordinating with quality, legal and authorities, ensuring timely submissions, and maintaining an obligations calendar with accountable owners.

Qualifications

• Hands-on Indian regulatory affairs experience in the actual product category being hired for.
• Evidence of submissions, claims or change-control work.
• Accurate documentation and cross-functional communication.
• Experience across multiple categories is welcome, but a candidate must not be expected to cover all possible pharma, FMCG and healthcare regimes alone.
• State product class and responsible legal entity on the live ad.

Responsibilities

• Own the regulatory workstream for specified India-based health, pharma or consumer products.
• Help the team understand which approvals, labels, claims and operating controls apply before a launch.
• Keep the compliance record current afterwards.
• Classify products and map applicable requirements.
• Prepare and track registrations, licences and renewals.
• Review labels, claims and promotional changes.
• Maintain evidence and an obligations calendar.
• Advise product and operations on changes.
• Coordinate with quality, legal and authorities within agreed responsibilities.
• Record and escalation gaps.

Job description

30 Health Centre of Excellence / Ziqsy Labs / regulatory

Regulatory Affairs Manager, India

Own the regulatory workstream for specified India-based health, pharma or consumer products. Help the team understand which approvals, labels, claims and operating controls apply before a launch, and keep the compliance record current afterwards.

The work

YOU WILL

• Classify products and map applicable requirements.
• Prepare and track registrations, licences and renewals.
• Review labels, claims and promotional changes.
• Maintain evidence and an obligations calendar.
• Advise product and operations on changes.
• Coordinate with quality, legal and authorities within agreed responsibilities.
• Record and escalation gaps.

YOU BRING

• Hands‑on Indian regulatory affairs experience in the actual product category being hired for.
• Evidence of submissions, claims or change‑control work.
• Accurate documentation and cross‑functional communication.
• Experience across multiple categories is welcome, but a candidate must not be expected to cover all possible pharma, FMCG and healthcare regimes alone.
• State product class and responsible legal entity on the live ad.

Good work looks like a clear obligations register, reviewed launch materials, timely submissions and known gaps with accountable owners and remediation dates.

What we cannot tell you yet.

Not one of these is settled for this role. Rather than guess, or hide them behind an Apply button, each gap says what has to happen before it closes.

Remote does not mean every country. Eligible hiring countries are set role by role, so tell us where you are and we will tell you straight away whether we can engage you there.