Regulatory Affairs Executive

Talish Solutions; Ahmedabad District; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Talish Solutions is seeking a Regulatory Affairs Executive with 3–5 years' experience in export formulations to lead ACTD/CTD dossier preparation, DMF review and ICH validation from Mumbai Fort. You will handle technical documentation and regulatory submissions across ROW, LATAM and Africa regions.

The role demands diligent coordination with third party and contract manufacturers to ensure timely approvals while maintaining strict compliance with global regulatory standards.

Qualifications

• 3-5 years' experience in Export Formulation.

Skills

ACTD/CTD

DMF review

ICH validation

Technical docs

Regulatory submissions

Education

B.Pharm

B.Sc

M.Pharma

MS/M.Sc

Job description

Executive - Regulatory Affairs. B.Pharm/M.Pharm with 3-5 years' experience in Export Formulation. Expertise in ACTD/CTD dossier preparation, DMF review, ICH validation, technical documentation, and ROW, LATAM & Africa regulatory submissions.

Role Category: Healthcare & Life Sciences - Other

Education

UG: B.Sc in Any Specialization, B.Pharma in Any Specialization

PG: MS/M.Sc(Science) in Any Specialization, M.Pharma in Any Specialization

Key Skills

Skills highlighted with '' are preferred keyskills

Third Party and Contract Manufacturing company of Pharmaceuticals, Nutraceuticals, Herbals Products.

Regulatory Affairs Executive - Fort ( Mumbai )