Regulatory Affairs Specialist Vacancies at Meril Life Sciences
Regulatory Affairs Specialist Hiring Alert Andheri (E), Mumbai
Are you passionate about maintaining the highest standards in medical device approvals and global regulatory compliance? Meril Life Sciences is seeking skilled Regulatory Affairs Specialists to join our International Regulatory Affairs department in Andheri (E), Mumbai. If you have 1 to 6 years of experience and a keen eye for detail, this opportunity is perfect for you.
About Meril Life Sciences
Company Overview
Meril Life Sciences is a leading medical device manufacturer dedicated to improving the quality of human life through innovative and reliable products. Our commitment to global healthcare standards and continuous improvement makes us a preferred employer in the industry.
Location: Andheri (E), Mumbai
Job Details
Regulatory Affairs Specialist
Position: Regulatory Affairs Specialist
Experience: 1 to 6 years
Location: Andheri (E), Mumbai
Work Schedule: 6 days a week (Mon-Sat)
Role Overview:
- Manage dossier submissions globally for medical devices.
- Coordinate device approvals with Ministries of Health and address related queries.
- Collaborate with R&D and Plant QA/RA for dossier compilation.
- Communicate with distributors and consultants worldwide to secure approvals.
- Assist in international registration with the Sales Team for country-specific registrations.
- Maintain and update submission records with precision.
- Prepare and monitor QMS documentation for audits based on individual country requirements.
Qualifications:
- Bachelor’s or Master’s degree Pharmacy or in a relevant field.
- 1 to 6 years of experience in regulatory affairs, preferably within the medical device industry.
- Excellent communication skills, both written and verbal.
- Strong attention to detail and ability to work in a dynamic, international setting.
- Proficiency in MS Office applications.
How to Apply
Interested Candidates
Please send your resume to akshay.revankar@merillife.com