Global ophthalmic medical device company Rayner is currently hiring a Vigilance Specialist in Ahmedabad, India. This opportunity is ideal for professionals with 3โ6 years of experience in pharmacovigilance, medical device vigilance, or post-market surveillance.
The role focuses on complaint handling, incident management, regulatory reporting, and compliance with global vigilance regulations. Professionals working in drug safety, regulatory affairs, or medical device safety can leverage this role to strengthen their expertise in global regulatory reporting and vigilance systems.
This position offers the chance to collaborate with global teams, regulatory authorities, and distributors, while contributing to patient safety and medical device compliance across international markets.
Job Overview
- Company: Rayner
- Role: Vigilance Specialist
- Location: Ahmedabad, India
- Department: Regulatory Affairs
- Job Type: Full-Time, Permanent
- Experience Required: 3โ6 years
- Industry: Medical Devices / Pharmacovigilance / Regulatory Affairs
This role is particularly suited for candidates experienced in medical device vigilance, pharmacovigilance case processing, complaint management, and post-market surveillance reporting.
Key Responsibilities
The Vigilance Specialist will manage end-to-end vigilance activities including complaint handling, safety reporting, and regulatory compliance.
Key duties include:
- Receiving, recording, evaluating, investigating, and processing complaints involving Rayner products.
- Managing complaint case workflows to meet internal and regulatory timelines.
- Conducting medical and technical evaluation of reported incidents.
- Maintaining accurate records in vigilance and complaint management systems.
- Preparing vigilance data for product risk management and global registrations.
- Supporting Clinical Evaluation Reports (CERs), Technical Files, and regulatory submissions.
- Submitting medical device incident reports to global regulatory authorities.
- Ensuring compliance with internal SOPs and international vigilance regulations.
- Assisting with SOP development, training materials, and vigilance documentation.
- Participating in internal audits, inspections, and compliance reviews.
- Acting as a liaison between distributors, regional teams, and global headquarters.
- Monitoring regulatory and legislative updates related to medical device vigilance.
Required Qualifications
Candidates applying for this Rayner Vigilance Specialist job in India should meet the following criteria:
Essential Requirements
- Bachelorโs degree in Life Sciences, Clinical Sciences, Engineering, or related field
- 3โ6 years of experience in:
- Pharmacovigilance
- Medical device vigilance
- Post-market surveillance
- Drug safety or complaint handling
Preferred Qualifications
- Postgraduate qualification in Pharmacovigilance, Regulatory Affairs, or Medical Device Vigilance
- Knowledge of global medical device vigilance systems
- Experience working with multiple regulatory authorities
- Prior experience with ophthalmic medical devices (preferred)
Skills Required
Successful candidates typically demonstrate:
- Strong knowledge of medical device vigilance regulations
- Experience in incident reporting and complaint investigations
- Familiarity with risk management and safety databases
- Excellent communication and stakeholder management skills
- Ability to collaborate with cross-functional global teams
Benefits and Perks
Rayner offers a competitive benefits package including:
- Health and wellness allowance
- Employee Assistance Program (EAP)
- Global recognition and appreciation platform
- Opportunity to work in a global medical technology organization
- Exposure to international regulatory markets and vigilance systems
Employees also contribute to improving vision and quality of life for millions of patients worldwide through Raynerโs ophthalmic innovations.
How to Apply
