Search Results: 2,790 vacancies
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...
...Description
MAIN PURPOSE OF ROLE
Specialist professional individual contributor with comprehensive knowledge in the area of Regulatory Affairs.
Ability to execute highly complex or specialized projects.
Adapts precedent and may make significant departures from...
...the Annual Report schedule.
Retaining all supporting documentation as required in completing an Annual Report.
Notifying Regulatory Affairs Manager or designee (and Quality, if required) that an Annual Report is at risk of being submitted late.
Decision Making:...
...event in Delhi 2022.
Responsibilities
Support in creating regulatory and quality policy plan as needed internally and externally
Work... ...Requirement
Good understanding of the latest regulatory affairs
Ability to quickly prioritize and execute tasks
Strong analytical...
...We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.
Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory Affairs
Experience: 3 to 9 years
Location: Andheri...
...database records pertaining to approved products in line with systems, processes and procedures.
Leading and/or coordinating regulatory affairs projects, as assigned.
Preparation of submission and approval notifications for applications submitted to Regulatory agencies...
...utilizing the electronic proofreading tool TVT.
Work with US Regulatory Labeling Team to ensure assigned projects like RLD updates, Safety... ...(Pharmaceutical industry experience, specifically in Regulatory Affairs with a focus on US Gx labeling
Knowledge and Skills...
...Organization for PE and BE studies.
Coordination with ANVISA for technical queries
Desired Skills
Complete knowledge of ANVISA regulatory guidance
Proficient in new product submissions for solid oral dosages, parental/sterile formulations to ANVISA
Reading/Writing...
...Lead consultant, Regulatory Affairs Pharmaceutical - LIF016391
Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility...
...intellectual firepower.
Welcome to the relentless pursuit of better.
Inviting applications for the role of a Lead consultant, Regulatory Affairs Pharmaceutical
You should have minimum years of experience in regulatory affairs with must knowledge of current regulatory...
...The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing...
...implementation of the change.
Co-ordination with GRA, Country regulatory affiliates and COE for submission of dossier and supporting the... ...you
Experience : (8-12 years of experience in Regulatory Affairs, Quality Assurance)
Soft skills : Transversal skills, Stakeholders...
...Responsibilities
Support in creating regulatory and quality policy plan as needed internally and externally
Work with internal personnel... ...to the candidate with 3+ years experience in regulatory affairs
Ability to quickly prioritize and execute tasks
Experience...
Pharmaceutical manufacturing company at Andheri East, Mumbai, having a vacancy for Regulatory Affairs.
B.Sc/B Pharma and should have experience as Regulatory Affairs in Pharma company
Job Profile: Regulatory Affairs & Compliance of Pharma company
Preparing dossiers...
...regulations.
To liaise with stakeholders to identify forthcoming regulatory challenges and proactively seek expert input to resolve issues... ...engagement.
Highly motivated and experienced regulatory affairs professional
Comfortable working with different cultures and...
Rs 2.2 - 2.8 lakhs p.a.
...checking and follow-up
Re-registration Dossier
Registration / Submission certificates updation
Translation files record
Regulatory Affair,Formulation,Pharmaceutical
Designation: Executive - Regulatory Affairs
Vacancies: 1
Experience: 1.0 Year(s) - 2.0 Year(s...
...# Responsible to provide CMC regulatory strategy as the CMC regulatory lead for drug substance and drug product during different clinical phases.
# Responsible for dossier/CMC document submissions timely by ensuring the complete contents. Provide support to maintain regulatory...
...we are embarking on an exciting journey to expand our reach globally.
Role and Responsibilities:
We are seeking a Manager Regulatory Affairs to join our team. In this role you will be responsible for supporting the creation of regulatory and quality policies both internally...
...Experience
Minimum 2 to 3 years relevant experience in handling Europe market.
Overall total experience in Regulatory of 3-5 years
Competencies
Good communication skills both spoken and written English.
Should be well versed with using excel sheets, Power Point...
...Regulatory lead will support in providing CMC strategy for drug substance and drug product during different clinical phases.
Responsible for product registration, approval and regulatory compliance throughout product life cycle.
The individual will be involved in CMC...
