Regulatory Affairs Specialist

Addictive Media; Raipur; On-site; INR 450,000 - 650,000; Full time

Job summary

Addictive Media in Raipur, Chhattisgarh invites applications for a Regulatory Affairs Executive to support export drug registration. The role combines hands-on dossier work with cross-team collaboration, under the Head of Regulatory Affairs, focusing on CTD/ACTD compilation and CDSCO documentation.

This on-site position offers immediate exposure to QA/QC and production data, learning from senior RA leaders, and a clear path to larger regulatory responsibilities as you grow.

Qualifications

• 0–4 years of experience in pharmaceutical regulatory affairs, quality, or a related pharma function.
• B.Pharm / M.Pharm or equivalent education is required.
• Freshers with a strong academic background are welcome to apply.
• Willingness to learn CTD/ACTD and work on-site in Raipur.

Responsibilities

• Support CTD/ACTD dossier compilation and documentation for export registration.
• Assist with CDSCO-related paperwork - WHO-GMP certification, COPP applications, export NOCs.
• Track registration status across export markets and flag pending items.
• Coordinate with QA/QC and plant teams to pull stability data, batch records, and COAs.
• Maintain organized, submission-ready documentation under the Head of RA's review.
• Learn end-to-end registration processes by working with senior RA and plant leadership.

Skills

CTD/ACTD documentation

Regulatory submissions

QA/QC coordination

Education

B.Pharm / M.Pharm or equivalent

Job description

Job Title: Regulatory Affairs Executive – Pharma Export (WHO-GMP / CDSCO)

Location: Raipur, Chhattisgarh (based close to our manufacturing facility)

Experience: 0–4 years

Employment Type: Full-time, on-site

The Role

We're hiring a Regulatory Affairs Executive to support our export drug registration process - working under our Head of Regulatory Affairs on CTD/ACTD dossier compilation, CDSCO documentation, and registration tracking across our active and target export markets. Being based at the plant means you're working directly with QA/QC and production to pull the data you need, rather than waiting on it over email.

This is a hands-on, learning-focused role - you'll be building real regulatory experience from day one, with senior support to guide you as you grow into bigger responsibilities.

What You’ll Do

• Support CTD/ACTD dossier compilation and documentation for export registration
• Assist with CDSCO-related paperwork - WHO-GMP certification, COPP applications, export NOCs
• Track registration status across our export markets (Africa, Middle East, CIS, South-East Asia) and flag what's pending
• Coordinate with QA/QC and plant teams to pull stability data, batch records, and COAs needed for submissions
• Maintain organized, submission-ready documentation under the Head of RA's review
• Learn the end-to-end registration process by working closely with senior RA and plant leadership

What You Bring

• 0–4 years of experience in pharmaceutical regulatory affairs, quality, or a related pharma function (freshers with a strong academic background are welcome to apply)
• B.Pharm / M.Pharm or equivalent
• Basic familiarity with CTD/ACTD documentation or willingness to learn quicklyComfortable working from Raipur, close to the manufacturing site
• Detail-oriented, organized, and reliable with documentation and deadlines

Why This Role

• Real, hands-on regulatory experience at a WHO-GMP certified export manufacturer - not a back-office desk job
• Being on-site at the plant means faster learning: direct access to QA/QC, production, and batch data instead of working at a distance
• Clear growth path into more senior regulatory responsibility as you prove yourself