Average salary: Rs295,000 /yearly
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...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...
...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...
...stakeholders
Compiling variation packages
Experienced in managing, regulatory database and Trackwise.
Your experience and qualifications... ....
Experience:
~2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market
~ Knowledge on...
...We are hiring for Regulatory Affairs Analyst IVD Expert
Your Role:
The Regulatory Affairs Analyst IVD Expert supports assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products.
Independently...
...Regulatory Affairs Consultant:
Around 7-10 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologicals) in various markets.
Good understanding of regulatory framework, including regional...
...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...
...Everyone at Halma India makes an impact, and so do you when you join us!
Responsibilities:
Have regular meetings with international Regulatory Teams of Halma Companies to understand their evolving business needs wrt Indian market.
Assist them in understanding the India...
...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...
...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...
*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...
...Associate Manager, Regulatory Affairs (CMC)
at ClinChoice (View all jobs)
Bangalore or Hyderabad - India
ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative...
...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...
...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...
...combination of this will lead to a truly differentiated experience for you.
If this excites you, then apply below.
Lead Regulatory Affairs
You will be responsible for :
Responsible for Regulatory intelligence dissemination and coordination, this includes
-...
~ B.Tech / BE , Graduate / Technical Graduate
3-5 years of experience in Regulatory affairs preferably in the medical device Industry.
Experience in EU MDR, US FDA, other global regulatory requirements. In depth understanding of ISO 13485, CFR 820, CE ISO 14971, certified...
...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...
...Regulatory Affairs Analyst is responsible for providing support in ensuring compliance with EU, US, and global medical device regulatory requirements
This position is primarily focused on supporting international registration requirements triggered by the EU Medical Device...
...Job Title
Senior Regulatory Affairs Specialist
Job Description
Job title: Senior Regulatory affairs specialist
Reports to: Regulatory Affairs Lead
Location: Bangalore
Position Summary:
The Regulatory Affairs Specialist supports and implements product...
...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
~...
