Average salary: Rs3,207,916 /yearly

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Search Results: 56,451 vacancies

 ...increasingly complex and stressed health system, Lilly Medical Affairs (MA) can provide clear, credible answers that will set Lilly apart...  ...; identifying patterns and trends in data sets; leveraging business intelligence and analytics (BI&A) tools to create actionable insights... 

Lilly

India
1 day ago
 ...and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit...  ...global registrations for assigned projects. · Collaborate with business unit and international regulatory affairs personnel to support marketing... 

Medtronic

India
4 days ago
 ...boundaries of science and technology. For the last 42 years, the combination of our purpose, strategy, people, DNA and sustainable business model has resulted in record long-term growth in revenues and profits and an increase in dividend by ≥ 5% every year– an achievement... 

Halma plc

India
5 hours agonew
 ...About the role Role Title: IT Business Analyst - Regulatory Affairs Location: Hyderabad About the Role: The job purpose is to act as a consultant and advisor providing guidance to improve complex global business processes, products, and services. We are looking... 
Hyderabad
more than 2 months ago
 ...aligned Clinical Scientist who plays a key role within the Medical Affairs organization. The primary focus of this role is to use the...  ...with the Brand team to meet both external customer and internal business needs. They lead to ensure all medical activities are in compliance... 

Lilly

India
4 days ago
 ...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... 

TECHNO ENDURA

Bangalore
6 days ago
 ...products. Responsibilities: •    Support daily Regulatory Affairs function eg; compliance to 21 CFR 820,807,803 ISO 13485 requirements...  ...respectfully to build positive relationships and improve business results. •    Ability to work effectively within a team in a fast... 

TE Connectivity

Bangalore
1 day ago
 ...About the job We are looking for an experienced Regulatory Affairs Specialist to join our growing team, to assist CMR Senior Regulatory...  ...develop existing processes by introducing efficiencies as our business grows Please use the below link for job application and quicker... 

Lifelancer

Mumbai
3 days ago
 ...and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit...  ...global registrations for assigned projects. · Collaborate with business unit and international regulatory affairs personnel to support marketing... 

Medtronic

India
4 days ago
 ...Manager Government Affairs Overview : Wipro Government Affairs has an opening for an experienced Global Government Affairs professional...  ...government agencies to enable the growth of organization’s business plans and interests in the global regions it operates. Celebrating... 
Delhi
2 days ago
Organisation : USV, a top -15 pharmaceutical company in India, excels in the diabetes and cardio sectors. With a presence in over 65 countries, our dynamic team of over 7,000 spans generations. Our commitment to brand building is evident in our popular products like Glycomet...

USV PRIVATE LIMITED

India
5 hours agonew
 ...Academic degree- and thinking level with a chemical/pharmaceutical background. Experience: ~2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market ~ Knowledge on registration procedures and pharmaceutical regulations ~ Interest and... 

Teva Pharmaceutical Industries Ltd

Bangalore
4 days ago
 ...the project team understand and work to the scope of the contract Identifies new opportunities through Change In Scope or add-on business from existing work Ensures timely project close-out activities are completed Consulting Activities and Relationship Management... 

Parexel

Bangalore
7 days ago
 ...of information, updates, and directives. Collaboration and Coordination: Collaborate with internal departments such as regulatory affairs, legal, compliance, quality assurance, and clinical operations to ensure alignment with regulatory requirements. Work with IP... 

Sanofi

India
1 day ago
 ...applications for the permits, licenses, certificates, authorizations, and other approvals that the organization needs to conduct its business activities; and produce, sell, and distribute its goods and services. These may include product licenses, manufacturing, import and export... 

Eastman

Hyderabad
9 days ago
 ...developments with the internal stakeholders Working closely with Business development to identify new molecules, novel drug delivery...  ...Engagement of identified key scientific leaders through medical affairs activities, in alignment with the overall franchise plan and create... 

Intas Pharmaceuticals

Ahmedabad
20 days ago
 ...If this excites you, then apply below. Lead Regulatory Affairs You will be responsible for : Responsible for Regulatory...  ...employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an... 

Indegene

Bangalore
23 days ago
 ...they define their priorities and policies. As Lead –Government Affairs BBU you will play a pivotal role in driving collaborations with...  ...leaders, including the AstraZeneca India country president and business unit director, to represent AstraZeneca’s Biopharmaceutical India... 

AstraZeneca

India
6 days ago
 ...they define their priorities and policies. As Manager – State Affairs you will play a pivotal role in driving collaborations with...  ...tools. Work directly with state  and BU leadership to implement business strategies in response to legislative/regulatory challenges and... 

AstraZeneca

India
6 days ago
 ...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... 

TECHNO ENDURA

Bangalore
8 days ago