Search Results: 18,918 vacancies
...Job Title: Regulatory Affairs Manager I (International Regulatory Affairs)
Career Level - D
Introduction to Role:
Within International Regulatory Affairs, as Regulatory professionals, we take innovative regulatory approaches to bring life-changing medicines to patients...
...Job Title: Regulatory Affairs Associate I (International Regulatory Affairs)
Career Level - C
Introduction to Role:
Within International Regulatory Affairs, as Regulatory professionals, we take innovative regulatory approaches to bring life-changing medicines to patients...
...Job Title: Regulatory Affairs Analyst Location: Bangalore
Job Type: Full-time
Years of Experience: 2-5
Company Description:
Our... ...safe and effective when used as advertised. Functioning as an internal regulatory board for an ISO 13485:2016 certified organization...
...necessary dossier changes in Europe and International Market
Responsible for compilation of... ...variation packages
Experienced in managing, regulatory database and Trackwise.
Your... ...5 years of experience in CMC Regulatory Affairs Mainly in Europe and International...
...necessary dossier changes in; Europe and International Market
Responsible for compilation of... ...packages
Experienced in managing, regulatory database and Trackwise.
Your experience... ...5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International...
...We are hiring for dynamic individuals in Regulatory Affairs Department:
Experience: 3 years up to 12 years
Designation: Senior Exec / Assistant Manager / Deputy Manager
Qualification: M. Sc. / M. Pharma/ B. Pharma
For Below Mentioned roles: -
Role 1: - API...
...Regulatory Affairs Specialist
Responsibilities:
Prepare and submit regulatory documentation for new and existing medical products, including... ...regulatory data.
Provide expert advice and guidance to internal teams on regulatory matters.
Manage and maintain...
...for you.
If this excites you, then apply below.
Lead Regulatory Affairs
You will be responsible for :
Responsible for... ...Familiarity with preparation and submission of 510 (k) , PMA or international documents or registration and marketing of medical devices worldwide...
...We are hiring for Regulatory Affairs Analyst IVD Expert
Your Role:
The Regulatory Affairs Analyst IVD Expert supports assigned regulatory... ...820, CMDR SOR 98-292, ISO 13485:2016, and other applicable International Medical Device Regulations is preferred.
Act as liaison...
...Regulatory Affairs Consultant:
Around 7-10 years of relevant experience in handling of pre and post approval life cycle management of drug... ...Type 2 meeting packages for USFDA and EMA
Co-ordination with internal and external stake holders for documentation required for...
...Regulatory Affairs Associate
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...
...This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ+ business community.
Regulatory Affairs Consultant.
~8 years' experience in handling life cycle management of approved drug products (small molecules) in various markets.
~ Good...
...Need another reason to apply? Here are 10 reasons to join our Regulatory Affairs/Quality Assurance team:
Who we want
Hard-working... ...Supporting new product development for both domestic and international release by contributing to the development and updating of regulatory...
...Job Description Summary
Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements... ...related Accessories. You will work within a team of Regulatory Affairs professionals to ensure GEHC establishes best practices in compliance...
...Graduate / Technical Graduate
3-5 years of experience in Regulatory affairs preferably in the medical device Industry.
Experience in... ...understanding of ISO 13485, CFR 820, CE ISO 14971, certified Internal Auditor.
Knowledge of ISO 13485 Quality management System,...
*Preparation and submission of Test License Applications(TLA) and Loan License Application (LLA)
*Preparation of NOC for TLA and LLA
*Coordination with functional departments, manufacturing sites
*Status updation of license applications and approval forms from DCK & CDSCO...
...our purpose to life. Everyone at Halma India makes an impact, and so do you when you join us!
Position Objective :
The Regulatory Affairs Specialist will be responsible with development, management, and implementation of regulatory strategies to support new and existing...
...and Responsibilities:
. With direction, develop and execute regulatory project plans
. Identify and elevate key areas of regulatory... ...and approve labeling and SOP's
. Represent or lead Regulatory Affairs in small project teams
Qualifications:
. Knowledge of regulations...
...them.
Job Description
Join our global team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating... ...and business development requests
Supervise Regulatory Affairs staff in the country
Qualifications
~ University degree
~...
...Product Regulatory Affairs (Life Sciences & Agriculture) work includes:
Directing submission development of product registration, progress reports, supplements, amendments, and/or periodic experience reports
Providing strategic product direction to teams on interaction...
