Current jobs related to Apsida Life Science | Regulatory Affairs Specialist | india - india - Apsida Life Science
-
Regulatory Affairs Director
3 days ago
India Apsida Life Science Full timeJob Description:Apsida Life Science seeks an experienced Regulatory Affairs Manager to lead our global regulatory submissions and ensure compliance with guidelines and company SOPs.About the Role:Deliver high-quality marketing, investigational, and lifecycle maintenance submissions within regulatory timelines and standards.Leverage in-depth knowledge of the...
-
Senior Regulatory Affairs Specialist
2 weeks ago
India Apsida Life Science Full timeApsida Life Science seeks an experienced Senior Regulatory Affairs Specialist to collaborate with our Global Regulatory Team Leads and submission teams. As a key member of our regulatory team, you will be responsible for ensuring timely and high-quality submissions that comply with global guidelines and company SOPs.The ideal candidate will have in-depth...
-
Apsida Life Science | Regulatory Affairs Manager
2 weeks ago
india Apsida Life Science Full timeRegulatory Submission Manager (Immediate start)Collaborate with Global Regulatory Team Leads, and submission teams to ensure timely, high-quality regulatory submissions that comply with global guidelines and company SOPs. Provide mentorship and training to team members, fostering excellence and first-time-right submissions.Responsibilities/Experience Deliver...
-
Regulatory Affairs Manager
2 weeks ago
India Apsida Life Science Full timeRegulatory Submission Manager (Immediate start) Collaborate with Global Regulatory Team Leads, and submission teams to ensure timely, high-quality regulatory submissions that comply with global guidelines and company SOPs. Provide mentorship and training to team members, fostering excellence and first-time-right submissions. Responsibilities/Experience...
-
Regulatory Affairs Manager
2 weeks ago
India Apsida Life Science Full timeRegulatory Submission Manager (Immediate start)Collaborate with Global Regulatory Team Leads, and submission teams to ensure timely, high-quality regulatory submissions that comply with global guidelines and company SOPs. Provide mentorship and training to team members, fostering excellence and first-time-right submissions.Responsibilities/Experience Deliver...
-
Regulatory Affairs Manager
2 weeks ago
India Apsida Life Science Full timeRegulatory Submission Manager (Immediate start) Collaborate with Global Regulatory Team Leads, and submission teams to ensure timely, high-quality regulatory submissions that comply with global guidelines and company SOPs. Provide mentorship and training to team members, fostering excellence and first-time-right submissions. Responsibilities/Experience ...
-
Regulatory Affairs Specialist
3 weeks ago
India Biocon Full timeAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Biocon in US/Canada Market. This role is an exciting opportunity for individuals with experience in formulation regulatory affairs.Key ResponsibilitiesPrepare, review and submit ANDA/ANDS in the US Market, including modules.Contribute to life cycle management for...
-
Regulatory Affairs Specialist
3 weeks ago
India BioTalent Search Private Limited Full timeJob Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Bengaluru. As a key member of our organization, you will play a vital role in ensuring compliance with regulatory requirements and driving the success of our medical device testing business.About Us:BioTalent Search Private Limited is a...
-
Regulatory Affairs Specialist
3 weeks ago
India ProPharma Full timeWe are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined operations...
-
Regulatory Affairs Specialist
3 weeks ago
India ProPharma Full timeWe are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined...
-
Senior Regulatory Affairs Specialist
2 weeks ago
India The Hird Full timeThe Hird is seeking a highly skilled Senior Regulatory Affairs Specialist to join our team in a remote location. This role offers a competitive salary of up to 19 LPA, with an estimated average annual compensation of 18.5 LPA.About the Role:We are looking for a seasoned professional with extensive experience in regulatory affairs and medical writing. As a...
-
india OMC Medical Limited Full timeRole Description This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...
-
india OMC Medical Limited Full timeRole Description This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...
-
ProPharma | Regulatory Affairs Specialist
3 weeks ago
india ProPharma Full timeWe are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined operations...
-
ProPharma | Regulatory Affairs Specialist
3 weeks ago
india ProPharma Full timeWe are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined...
-
Regulatory Affairs Specialist
3 weeks ago
India OMC Medical Limited Full timeAbout the RoleThis is a full-time on-site position for a Regulatory Affairs Associate at OMC Medical Limited. The successful candidate will be responsible for handling regulatory documentation, ensuring regulatory compliance with medical devices and cosmetics regulations, and managing overall regulatory affairs.Key ResponsibilitiesPreparing and reviewing...
-
india FLOAID MEDTECH Full timeLocation: IIT Madras Research park, Chennai, India Position Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time) Salary: Based on Experience Company Overview We, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to...
-
India ProPharma Full timeWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProPharma on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined operations within Veeva Vault.Key ResponsibilitiesData Reconciliation and...
-
india FLOAID MEDTECH Full timeLocation: IIT Madras Research park, Chennai, IndiaPosition Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time)Salary: Based on ExperienceCompany OverviewWe, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to provide...
-
India B. Braun Medical Inc. Full time**Job Description**: You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping...
Apsida Life Science | Regulatory Affairs Specialist | india
2 months ago
Apsida Life Science are looking for a Regulatory Affairs Specialist for a long term project.
Immediate start
You will need to
- Provide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams.
- Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia, Singapore and other ROW countries.
- Oversee product and GMP registrations, compile submission packages, and collaborate with internal teams to address any documentation needs.
- Engage closely with Marketing, Trade Marketing, Innovation, Industrial Affairs, Medical, Supply Chain, Pharmacovigilance, and Quality teams to provide integrated regulatory support.
- Serve as the main contact for MAT-related issues, managing escalations with Local and Global Regulatory Affairs, and external partners.
- Facilitate translation requests, artwork finalization, and certificate management for submissions.
