Average salary: Rs360,000 /yearly
More statsSearch Results: 15,668 vacancies
...Medical Device Regulatory Affairs Job duties of a Regulatory Affairs Specialist include:
Developing and implementing regulatory strategies for new and existing products
Preparing and submitting regulatory documentation to regulatory authorities
Liaising with regulatory...
About the job
Key Accountabilities:
Project Execution:
Works effectively within a team environment
Works within broad project guidelines as directed by the Project Lead or Technical SME
With the guidance of the project Technical SME, demonstrates the ability ...
.... Dispatch of registration dossiers to the National Drug
Regulatory Authorities (NDRA)/agents as applicable.
6. Actively finding... .... Knowledge of ROW market and regulatory experience in medical devices is preferred.
Contact Person:
Rina Arun / Srushti raval...
Dear Candidates, Greetings from Randstad India ! We have an opening for the role of Executive - Regulatory Affairs with a leading pharma company in India. Interested candidates can drop your resume to the mail id ****@*****.*** The details are below: Qualification...
...Job description
The Director of Regulatory Affairs at DELFI Diagnostics will support the representation of DELFI with the FDA and other... ...activities, implementation, and compliance experience in the medical device industry. 5+ years of medical device software experience,...
Rs 2.2 - 2.8 lakhs p.a.
...checking and follow-up
Re-registration Dossier
Registration / Submission certificates updation
Translation files record
Regulatory Affair,Formulation,Pharmaceutical
Designation: Executive - Regulatory Affairs
Vacancies: 1
Experience: 1.0 Year(s) - 2.0 Year(s...
...Lead consultant, Regulatory Affairs Pharmaceutical - LIF016236
With a startup spirit and 115,000 + curious and courageous minds, we have the expertise to go deep with the world’s biggest brands—and we have fun doing it! We dream in digital, dare in reality, and reinvent the...
Rs 3 lakh p.a.
...Analytical method validation review as per the ICH guideline.
- Drug Master File review
- Technical query response to the various regulatory authorities.
Ideal Profile
~ You have at least 1 year post-qualification experience in a similar role.
What's on Offer?...
Rs 5 - 6 lakhs p.a.
...work frequently with other employees and team members to coordinate complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory Responsibility means a duty or responsibility, assigned to an individual by...
...with cross-functional teams to implement regulatory initiatives and quality improvement... ...internal departments such as regulatory affairs, legal, compliance, quality assurance, and... ...extraordinary Better is out there. Better medications, better outcomes, better science. But...
...suitability for specific territories.
Regulatory strategize, prepare and submit MAAs to Medis... ...to 18 years of experience in Regulatory Affairs
~ Expertise in global regulatory... ...color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity...
...Job Description
Job Title: Regulatory Affairs Director
Career Level - F
Introduction to Role: Are you ready to apply your Regulatory Affairs strategy expertise to make a real difference? At AstraZeneca, we follow the science and turn ideas into life changing medicines...
Hi Greetings from Randstad we are hiring for Regulatory affairs specialist - IDMP Responsibilities : Lead/manage XEVMPD/IDMP submissions creation maintenance and their QC and
Compliance and All other XEVMPD/IDMP related activities.
- Responsible for tracking and communicating...
Rs 2 - 5 lakhs p.a.
...dossier of as per current prescribed guidelines of the respective regulatory authority.
~ Well versed with the guidelines of ICH and... ...record of dossiers, samples legal documents.
RA,Regulatory Affairs
Designation: Officer / Executive - Regulatory Affairs
Vacancies...
...around the world. We support pharmaceutical, biotechnology, and medical device companies with the services needed to perform clinical trials... ...day.
Job Description
You will focus on leading regulatory services for global research projects of novel medicinal products...
...Regulatory affairs officers ensure that products such as foods, cosmetics, pharmaceuticals and veterinary medicines and the steps involved... ...in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials . They are often...
...Regulatory Affairs Specialist
Responsibilities:
Prepare and submit regulatory documentation for new and existing medical products, including drugs, devices, and biologics.
Stay up-to-date on ever-evolving regulatory requirements and guidelines.
Liaise with regulatory...
Rs 10 - 15 lakhs p.a.
...product application (ANDA/EU-MA)/Post approval submission to the regulatory authority (specifically EU/US)
-Hand on experience in... ...hand Ons experience for handling of E-CTD software
Regulatory Affair,RA
Designation: Regulatory Affairs - Pharma
Vacancies: 1...
Rs 3 - 5.5 lakhs p.a.
...Description :
Regulatory Compliance:
Stay updated on medical device regulations, standards, and guidelines (e.g., FDA, ISO, CE Marking).
Ensure that products... ...or Biomedical Engineering or Diploma in Regulator Affairs, Quality Management System.
~3-5 years of...
$ 70000 p.a.
...ll meet these challenges. Join us!
The Senior Director, Regulatory Affairs is a leader, who provides vision and direction in a fast-paced... ...benefits package that includes stock options, annual bonus, premium medical, dental, and vision coverage for employees and their...
