Average salary: Rs1,186,132 /yearly
More statsSearch Results: 14,008 vacancies
...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...
...Job Title: Regulatory Affairs Specialist
Company: MakroCare
Location: Hyderabad Telangana (Onsite)
Company Description:
MakroCare is a leading provider of regulatory and clinical development solutions based in Hyderabad Telangana. We specialize in offering comprehensive...
...Basic understating about ISO 13485 and US FDA regulation (Medical Device Related)
Qualifications & experience:
Relevant regulatory and quality assurance experiences in international company for 2 years
Physical & mental requirements:
Detailed oriented....
(JOINING ASAP) We are seeking for a Regulatory Affairs Specialist who will be responsible for ensuring the delivery of regulatory activities performed in the platform/hub: About us
Responsibilities
To contribute to the production of client administrative documents...
...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...
...We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team.
Positions are: Executive / Sr. Executive / Asst. Manager - Regulatory Affairs
Experience: 3 to 9 years
Location:...
...Job Description
Job Title - Regulatory Affair Manager
Career Level : C
Lead the way for a new breed of solutions-oriented Regulators... ...THE ROLE The Regulatory Affairs Manager I is a regulatory specialist with project management capabilities responsible for leading...
...About the job
We are looking for an experienced Regulatory Affairs Specialist to join our growing team to assist CMR Senior Regulatory Affairs Specialist (AMEA) in all tasks relating to registrations for new or modified product. We are advertising this role to be based...
...authorities deficiency
Scientific Advice
Variations and Supplements (Type IA, IA, Type IB Type
Timely review of technical and regulatory documents i.e. Specifications, batch records, method validation documents, Stability data, container closure system, DMF review....
...Job Description
Job Title: iCMC Regulatory Affairs Manager
Career Level - D
Introduction to Role:
Join our Biopharmaceuticals... ...safe environment, where you will be part of a team with deep specialist knowledge and regulatory expertise. We are confident in what...
...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...
...-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 submissions...
...difference with.
The opportunity
To organize and perform required regulatory tasks in order to maintain existing EU procedures in line with... ...duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel.
Awareness of current/pending regulatory...
Rs 3 lakh p.a.
...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 similar role.
What's on Offer?...
...What are the Key Deliverables in this role ? Financial Outcomes
Minimize financial impact of regulatory changes to Business through various actions/choices responses.
Identify and optimize financial implications of regulatory components on product, packaging and promotions...
...Position : Executive Department : Regulatory Affairs - Formulation
Location : Kandivali - West, Mumbai
Qualification - M Sc/ B Pharm/ M Pharm
Experience : 4 - 8 years and above
Role
Responsible for activities related to own submission and support...
...Position: Intern, R&D - Regulatory Affairs Intern Qualification: (2022, 2023 & 2024) B.Pharm / M.Pharm
Duration: 12 months
CTA: Depending on performance maybe be converted into full time resources at the end of the internship period
Work Timing, General Shift:...
...This position provides medical and scientific expertise for regulatory submissions and implies in-depth expertise within medical science... ...(TACT templates) .
Cross-functional focal point for medical affairs issues raised through deficiency letters of Gx and innovative products...
...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 regulatory...
...: Duties & Responsibilities
Project Management:
Support Regulatory projects and Compliance standpoint on key projects within EM Regulatory... ....
Years of Experience: at least 7 years in Regulatory Affairs & RA compliance, data analysis, project Management …
Language:...
