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) - 8 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 - 3 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 - 9 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 - 14 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 - 18 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 - 17 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 - 25 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 - 29 days ago
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