Regulatory Affairs Jobs in Pune

Philips - Pune, Maharashtra, India

Job Title Associate Director Regulatory Affairs MoS Job Description Associate Director Regulatory Affairs MoS Critical RA leader of the IGTS MoS Category (Image Guided Therapy Systems Mobile Surgery

from: jobleads.co.in (+1 source) - 7 days ago

Right Advisors Private Limited - Pune

to routine activities and updation.Any other work assigned by supervisor. Designation: Sr executive/Assistant Manager - Regulatory Affairs Vacancies: 1 Experience: 5.0 Year(s) - 10.0 Year(s) 10.00 LPA To 12.00 LPA INR

from: jobitus.com - More than 30 days ago

Pune, Maharashtra, India

to ensure adequate availability of necessary medical supplies and equipment. Compliance and Regulatory Affairs: Ensure compliance with all relevant healthcare regulations and accreditation standards. Keep

from: jobleads.co.in - More than 30 days ago

Emcure - Pune

Role: Regulatory Affairs Canada Job location: Pune, Wakad Experience: 4-10 Years JD : 1. Experience in Canada market is required 2. Involved in Dossier preparation, Submission, Compilation of NDS Not disclosed INR

from: naukri.com - 2 days ago

TECHNO ENDURA - Bangalore,Chennai,Hyderabad,Pune,Mumbai City

Regulatory Affairs Associate Job duties of a Regulatory Affairs Specialist include: Developing and implementing regulatory strategies for new and existing products Preparing and submitting

from: Shine.com - 8 days ago

Randstad MENA - Pune (Maharashtra)

India! We have an opening for the role of Assistant Manager - Regulatory Affairs with a leading pharma company in India. Interested candidates can drop your resume to the mail id celci.w@randstad.in

from: timesjobs.com - 13 days ago

TECHNO ENDURA - Bangalore,Chennai,Noida,Hyderabad,Kolkata,Gurugram,Pune,Mumbai City,Delhi

Regulatory Affairs Specialist Job Description Responsibilities: Prepare and submit regulatory documentation for new and existing medical products,including drugs,devices,and biologics. Stay up

from: Shine.com - 17 days ago

Randstad - Pune

Market: EU . Review of compilation of submissions,deficiencies and post approval variations Experience: 6-10 Years. Not disclosed INR

from: naukri.com - 16 days ago

Fresenius Kabi - Pune

Preparation and submission of documents required post approval variations for FK Products (Pharma and Medical Devices) in India and overseas markets Knowledge of D&C Acts and Rules is must Not disclosed INR

from: naukri.com - 24 days ago

Acesso Innovation Lab - Other Maharashtra,Pune

and guidelines. Collaboration and Communication: Collaborate closely with cross-functional teams, including clinical operations, pharmacology, and regulatory affairs, to support study objectives. Communicate

from: Shine.com - 28 days ago