Average salary: Rs546,666 /yearly
More statsSearch Results: 14,602 vacancies
...in Gandhidham and Corporate office in Ahmedabad
Position : Regulatory Officer
Job Location : Bodakdev (Ahmedabad)
Reports To... ....
5. Dispatch of registration dossiers to the National Drug Regulatory Authorities (NDRA)/agents as applicable.
6. Actively...
...Job Title: Regulatory Affairs Analyst Location: Bangalore
Job Type: Full-time
Years of Experience: 2-5
Company Description:
Our client, Origin Medical is a healthcare technology company that aims to democratize quality prenatal care globally. The company provides...
...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...
Rs 10000 - Rs 25000 per month
...We are hiring for Regulatory Affairs Executive. Qualification: B.pharm/M.pharm
Age criteria: below 30
Experience - 0 to 2 years only
Location - Sola, Ahmedabad
Work mode - on site
:
Should have worked in Regulated Market (ROW).
Dossier Submission, Dossier...
QUALIFICATIONS:-
B.PHARMA / M.PHARMA
PHARMA REGULATORY
Skills
Analytical
~ Time management
Presentation skills .
Interpersonal... ....
Experience-- 4-5 Years of Experience in Pharma Regulatory Affairs
Job Summary
Core understanding of technical requirements...
...We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility... ...the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate...
...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...
Key Deliverables
Dossier review and complication of ANDAs for US Market.
Post approval for US
Document review i.e. Specifications, batch records, method validation documents, Stability data, container closure system, DMF review.
Hands on Electronic Operation (eCTD...
...validations preparation & review.
Analytical method validation review as per the ICH guideline.
Drug Master File review
Technical query response to the various regulatory authorities.
Ideal Profile
~ You have at least 1 year post-qualification experience in a...
...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...
...stakeholders
Compiling variation packages
Experienced in managing, regulatory database and Trackwise.
Your experience and... ....
Experience:
~2-5 years of experience in CMC Regulatory Affairs Mainly in Europe and International Market
~ Knowledge on registration...
...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...
...Pharmacy, pharmacology, Biotechnology, engineering, or medical technology.
Minimum 5 years of experience in Medical devices regulatory affairs and 7-8 years of working
experience in a Medical devices/Pharmaceutical company.
Good working knowledge of MS-EXCEL and PowerPoint...
...and organizational success.He/she measures success against the best internal and external benchmarks.
What you will do
Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies Participates in advocacy activities...
...Job Title: Regulatory Affairs Manager  Â
As the Regulatory Affairs Manager, you will play a crucial role in ensuring compliance with regulatory... ...regulatory documents for product registrations, including New Drug Applications (NDAs), Marketing Authorization Applications (...
...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...
...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 understanding of regulatory...
...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
-...
...artwork of packaging materials as per current rules and regulations.
Must have worked on ASEAN, CIS, and AFRICA markets.
Review all regulatory agency submission materials for accuracy, comprehensiveness, or compliance with regulatory standards
Evaluation of change...
JOB DESCRIPTION
Job Title
Regulatory Affairs Manager
Job Description
Job Description
Business Title: Manager - Regulatory affaire
In this role, you have the opportunity to make life better.
Looking at the challenges the world is facing today Philips...
