Regulatory documentation affairs

Relocation Assistance Offered Within Country Mumbai, Maharashtra, IndiaWho We AreColgate-Palmolive Company is a caring, innovative growth company that is reimagining a healthier future for all people, their pets and our planet. Focused on Oral Care, Personal Care, Home Care and Pet Nutrition, we sell our products in more than 200 countries and territories...

We are seeking a detail-oriented and proactive Assistant Manager for Regulatory Affairs to join our team. The role involves preparing, reviewing and submitting regulatory documents aligned with Dossier preparation for CIS, Asian and African countries. The ideal candidate should have a strong knowledge of regulatory frameworks and experience in the...

Requisition ID Posted 10/06/2025 - Research & Development - India - Maharashtra - Mumbai - Colgate-Palmolive - Travel - up to 10% of time - On-siteRelocation Assistance Offered Within Country Mumbai, Maharashtra, IndiaWho We AreColgate-Palmolive Company is a caring, innovative growth company that is reimagining a healthier future for all people, their pets...

We are seeking an experienced and detail-oriented Executive Regulatory Affairs (ROW) to join our Regulatory team. The ideal candidate will be responsible for preparing, reviewing, and submitting dossiers for semi-regulated and non-regulated markets, ensuring compliance with global regulatory requirements, and coordinating with internal departments and...

You will be working as an Asst Manager / Manager in the Biologics function of USV Private Limited in the Regulatory Affairs department specifically focusing on Clinical Trials for the EU and US markets. Your role will involve the following key responsibilities: - Developing Biosimilar Clinical Development Strategy, focusing on clinical trials and injectables...

Cliniminds is hiring Senior Associate Regulatory Affairs on behalf of globsl consulting company.Role Summary:The Senior Regulatory Associate plays a key role in supporting regulatory submission activities across Asian markets, primarily for biosimilar products. This role involves hands-on drafting, quality checking (QC), and performing Level 1 review of eCTD...

Designation: Senior Executive Regulatory Affairs & QAJob Profile:Responsible for registration of Pharmaceutical, Nutraceutical, Cosmetic products especially in international markets like ROW, MENA, SEA, LATAM etc.Compile, Review & Submit the Dossiers to the Distributors as per the MOH guidelines.Coordinating & follow-up up with the suppliers and distributors...

One of our esteemed Pharma client based at Mumbai is looking for AVP/VP Regulatory Affairs for US Markets. Job Description is given below;Job Description – Vice President (VP) Regulatory AffairsIndustry:Pharmaceutical ManufacturingLocation: MumbaiExperience:20+ yearsQualification:BPharm/M.Pharm / Ph.D. in Pharmaceutical SciencesRole OverviewWe are seeking...

Company :Founded in 1758 in Grasse in the south of France, Maison Sozio is one of the pioneers in fine French perfumery.The history of the Maison Sozio goes back to one of the very first families of perfumers in Grasse, having been at the origin of the community of glove-makers and perfumers.With the integration of Synarome in 2021, Sozio ties back to its...

UMEDICA is a vertically integrated company engaged in the manufacturing and export of a wide range of finished formulations i.e., Tablets, Capsules, Suspensions, Dry Syrups and SVP, at UMEDICA's manufacturing facility, located in Vapi (Gujarat). Facility is accredited by global regulatory agencies like EU, PICs, Local FDA and Inspected by USFDA.UMEDICA was...