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...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...
...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...
...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...
...Manager – Global Regulatory Affairs Location – Head-Office, Bangalore, IN
BIOCON BIOLOGICS
Biocon Biologics, we are creating a model for the future of healthcare for all. We are a leading company in the biosimilars revolution where patients come first. Our ambition...
...Regulatory affairs officers ensure that products such as foods, cosmetics, pharmaceuticals and veterinary medicines and the steps involved in developing, testing and marketing them meet legislative requirements. Typical duties include: studying scientific and legal documents...
...being – a fundamental driver for many of us to show up and do our best each day.
Job Description
You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics...
...safer, sustainable and more connected world.
Job Overview
Regulatory Affairs oversees compliance activities for customers. This covers... ...products.
Responsibilities:
• Support daily Regulatory Affairs function eg; compliance to 21 CFR 820,807,803 ISO 13485...
...Associate Manager, Regulatory Affairs (CMC)
at ClinChoice (View all jobs)
Bangalore or Hyderabad - India
ClinChoice is a global full-... ...years of experience in Medical, Clinical & Regulatory writing in Pharma & Medical Devices space.
Should have at least 5+ years of...
...the job
Job Description Summary
This position is responsible for the creation, identification, collection, and entry of regulatory affairs information of medical devices. Support related regulatory affairs activities, such as assessment, execution and management of...
...proven end to end expertise from clone development, manufacturing, clinical development, regulatory approvals to commercialization in developed and emerging markets. Global Regulatory Affairs
The Global Regulatory Affairs (GRA) at Biocon consists pool of talented...
...Department:
Regulatory Affairs CMC & Device
Are you passionate about what you are doing? Do you want to build excellence within processes... ...in related field along with Graduate or Post Graduate Degree Pharma, Biomedical and Engineering graduates preferred.
-Experience...
...experienced professionals associated with key regulatory processes covering CMC, Medical Device... ...CAPA) cases, and representing Regulatory Affairs in audits and core groups for device... ...-A Graduate or Post Graduate Degree in Pharma, Biomedical and Engineering graduates preferred...
....
Department: Regulatory Affairs Rare Blood Disorders
Job Level: 6
Are you passionate about driving regulatory strategy and life cycle management of product portfolio ensuring interactions with regulatory authorities across the globe? Do you thrive in a multi-...
...Department: International Operations Regulatory Affairs Bangalore
Are you experienced in project management? Do you thrive in a fast-paced and dynamic environment? We are looking for a Regulatory Project Manager to join our IO Regulatory Affairs team in Bangalore....
...hand as there is an exciting opportunity waiting for you as “CMC Regulatory Professional II” with us. "Apply now" - At Novo Nordisk, we... ...will experience the best.
About the department
Regulatory Affairs plays an important role in ensuring all Novo Nordisk Medicines and...
...Department : RA Labelling
Are you passionate about ensuring regulatory compliance and driving high-quality global packaging materials?... ...join our team in Bangalore and be part of our global Regulatory Affairs (RA) hub. If you are ready for a challenging and rewarding...
...hybrid environment, Apply now!
The Position :
As a Senior Regulatory Professional, you are expected to demonstrate leadership quality... .... The objective of the team is to offer core Regulatory Affairs (RA) competencies enabling Novo Nordisk (NN) to secure fast, high...
...our team today!
The purpose of Associate Manager, Global CMC Regulatory, is to work cross functionally with Elanco manufacturing and quality... ...Core Competencies:
~1 to 3 years in Global Regulatory Affairs, preferably within Post-approval CMC Life Cycle Management.
~...
Making financial projections : Pharmaceutical consultants help clients forecast how much drug development projects will cost and how to cover those expenses. Identifying operational problems: Reviewing business data and identifying problems is one of the central duties of ...
...your hand as there is an exciting opportunity waiting for you as “Regulatory Professional II” with us. "Apply now" - At Novo Nordisk, we... ...Qualification
~7-8 years of experience within Regulatory affairs with Graduate /
~ Postgraduate degree in Life-Science/ Chemistry...