Average salary: Rs625,000 /yearly
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...guidance to improve complex global business processes, products, and services. We are looking for an experienced individual in GDD Regulatory Affairs to lead the business analysis activities for the solutions that re-define how Novartis operates. You will be working on...
...exploring candidates with a less traditional background.
Job Description
Job Summary
We are looking for a seasoned Head Regulatory Affairs to lead the regulatory strategy, ensuring compliance with health product regulations and fostering organizational growth through...
...the development and implementing the effectiveness of the robust regulatory strategy and plans for
projects in development and approved,... ...to identify unique opportunities.
Sound understanding of the drug development continuum with thorough knowledge of regulatory approval...
...launches; private equity fund administration; advisory firm set-up, regulatory registration and infrastructure design; ongoing regulatory... ...Responsibilities
The Senior Associate: Enterprise Risk and Regulatory Affairs will provide support:
to the attainment of the overall...
...Position Overview:
The Manager of regulatory and Strategic Development will be responsible for developing and implementing and regulatory... ...strategic development submission management and regulatory affairs programs.
Develop and execute on global strategic plans (regulatory...
...Regulatory CMC, Regulatory Delivery Excellence leads, in partnership with the GRA-CMC RA Scientists, the various aspects of global marketing... ...internal forums to continue to develop and share regulatory and drug development expertise to meet critical product registration...
...and drive innovative solutions.
We are looking for a Sr. Regulatory Affairs / Regulatory Intelligence Associate (Pharmaceutical and... ...policies issued by regulatory authorities, such as the FDA (Food and Drug Administration), EMA (European Medicines Agency), and other...
...- CTD Dossier Drafting (Modules 2, 3, 4)
- Regulatory writing
- Clinical Regulatory Pharmacovigilance Regulatory
- Preparation of Tox applications, CTAs, MAAs
- Regulatory commitment compliance
- Any other Regulatory activities on need basis
- Support Line...
About the Role
Role Title: Sr. Spec. DDIT Dev. Technical Design (Regulatory Affairs)
Location: Hyderabad
Role Purpose:
The purpose of the role is to
• Lead the design and managing deliverables of RA Publishing business critical applications as well as provide support...
Join the fastest growing Generic company specializing in Injectables, Oncology, Ophthalmic & hormones
Join our team as an Executive, Sr. Executive, Asst. Manager or Deputy Manager
Be a part of our success story!!!
We have openings for the following positions:
Exp...
...timely submission. Independently manage US regulatory compliance activities, including timely... ...requests. Independently manage and execute drug shipment ticket review process (US)
In... ...Development
Business Unit
REG AFFAIRS GDD
Work Location
Hyderabad, AP...
...Department : Regulatory Affairs, US Market
Role : Labeling
Experience : 2-8 years
Qualification : B. Pharm/M. Pharm
Job Description... ...artworks and print proofs of commercial labeling on Agile.
- Drug Listing for the approved ANDAs.
- Review and Approval of...
...downstream process development for Biotherapeutics/ Biosimilars. Current trends in the Biopharma industrry and good understanding of regulatory framework and IP landscape. Prior experience on the ADCs process development will be prefered.
Additional Information...
Requirements:
Creating talent acquisition strategies based on the client requirement and ensuring fulfillment with speed and quality of pipeline generated.
Provide talent insights and talent landscape to the clients
Advising clients on the talent availability and effective...
...information into intelligence, inspiring the world to learn, communicate and advance faster than ever.
JR51354 Government and Public Affairs Manager
Job Description for Government and Public Affairs Manager
Micron Technology's vision is to transform how the world...
...Role Description
This is a full-time on-site role for a Director Academic Affairs (Social Sciences) at Woxsen University located in Hyderabad. The Director Academic Affairs will be responsible for overseeing the academic programs and faculty within the Social Sciences...
...Department : Regulatory Affairs, US Market
Role : Post Approval
Experience : 2-8 years
Qualification : B. Pharm/M. Pharm
Job Description :
- Planning, reviewing and submission for assigned ANDA and NDA projects within timelines.
- Adherence to high quality,...
...culture products (Biosimilars) in defined terms of volumes and timelines, while ensuring compliance to quality standards, GMP and other regulatory and statutory requirements, as per schedule.
3. mandatoriy to have cGMP and knowledge of safety. Quality Systems - For Downstream...
Implement global category strategy at local level OR implement sourcing business plan for area of responsibility; directly deploys global category strategy at site level.
Supervise the implementation of sourcing plans for the sub-category deliver sub-category savings targets...
1.Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc. 2. Performs quality control (QC) checking / proof reading of the above mentioned...
