Regulatory Affairs Jobs in Thane

Encube Ethicals - Mumbai, Maharashtra, India (+1 location)

Document review i.e. Specifications, batch records, method validation documents, Stability data, container closure system, DMF review. Hands on Electronic Operation (eCTD and SPL) Understanding labelling...

from: linkedin.com (+1 source) - 6 days ago

Unichem Laboratories Limited - Mumbai, Maharashtra, India

Compilation of ANDA submissions in accordance with the latest guidances assuring technical congruency and regulatory compliance. Identify the required documentation for EU regulatory submissions and compilation...

from: linkedin.com - 6 days ago

Double HR Consultancy - Vile Parle East Mumbai

VACANCY REGULATORY AFFAIRS EXECUTIVE (Pharma Company is manufacturing veterinary products) Job Location: Mumbai Maharashtra Eligibility : M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma

from: placementindia.com - 3 days ago

Unichem Laboratories Limited - Mumbai, Maharashtra, India

Qualifications : B.Pharm/ M. Pharm/ M.Sc. Location: For two years in Brazil Office followed by Office in Mumbai Job description Responsibilities Ensure change management, post approval changes

from: linkedin.com - 9 days ago

Meril - Mumbai, Maharashtra, India

We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team. Job Titles: Executive / Senior Executive / Assistant

from: linkedin.com - 19 days ago

Rubicon Research - Thane

Should have experience in dossier preparation,submission,query responses and registration in regulated countries Not disclosed INR

from: naukri.com - 25 days ago

KlinEra Global Services - Mumbai, Maharashtra, India

The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play

from: linkedin.com - More than 30 days ago

Wellbeing Nutrition - Mumbai, Maharashtra, India

years in regulatory affairs (FSSAI, AYUSH, FDA) and 2-3 years in nutraceutical product development. DESIRABLE: M.Sc. (Nutraceutical) & A regulatory certificate course

from: linkedin.com - 7 days ago

Rubicon Research - Thane

Review specifications,batch manufacturing,process validation,method validation,and analytical documents for submissions USFDA Experience . Not disclosed INR

from: naukri.com - 26 days ago

Bharat Serums and Vaccines Limited - Navi Mumbai, Maharashtra, India

, contribute to Medical review/input to clinical trial documents/activities and regulatory documents/ applications. Lead planning, preparation and execution of Medical affairs strategies and plans for Key

from: linkedin.com - 6 days ago