Rayner Hiring Vigilance Specialist
- Rayner Hiring Vigilance Specialist India | Pharmacovigilance Jobs Ahmedabad | Apply Now
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Qualification:
- Experience:
- Preferred Qualifications:
- Skills Required:
- Location & Salary
- Application Process
- Why Join Rayner?
- Frequently Asked Questions (FAQs)
- 1. What experience is required for this role?
- 2. Is medical device experience mandatory?
- 3. What qualifications are required?
- 4. What is the job location?
- 5. What type of work will I handle?
- Summary Table
Rayner Hiring Vigilance Specialist India | Pharmacovigilance Jobs Ahmedabad | Apply Now
Rayner is hiring experienced professionals for the role of Vigilance Specialist in Ahmedabad, India. This full-time position focuses on end-to-end complaint handling, medical device vigilance, regulatory reporting, and post-market surveillance activities. The role is ideal for candidates with 3–6 years of experience in pharmacovigilance, medical device vigilance, or regulatory affairs.
This opportunity offers exposure to global regulatory systems, complaint management workflows, and safety reporting for medical devices, making it highly relevant for professionals aiming to grow in drug safety, pharmacovigilance, and regulatory compliance careers.
Company Overview
Rayner is a globally recognized medical device company specializing in ophthalmology products, particularly intraocular lenses and surgical solutions. With a strong legacy of innovation and patient-focused healthcare solutions, Rayner plays a critical role in improving vision outcomes worldwide.
The company operates across multiple international markets and maintains strict compliance with global regulatory standards. Rayner’s vigilance and safety systems ensure product quality, patient safety, and regulatory adherence across all regions.
Working at Rayner provides an opportunity to contribute directly to patient safety and global healthcare advancements through robust vigilance and compliance systems.
Job Role & Responsibilities
As a Vigilance Specialist, you will be responsible for managing complaint handling and safety reporting processes for medical devices across global markets.
Key Responsibilities:
- Receive, record, evaluate, and investigate complaints related to marketed products
- Manage complaint workflows to meet internal and regulatory timelines
- Perform medical and technical evaluation of adverse events
- Maintain accurate documentation in vigilance and complaint management systems
- Prepare vigilance data for product risk management and regulatory submissions
- Support global registrations through safety data and compliance documentation
- Contribute to Clinical Evaluation Reports, Technical Files, and regulatory dossiers
- Submit incident reports to global health authorities
- Ensure compliance with SOPs and international vigilance regulations
- Support training of stakeholders on vigilance processes and compliance requirements
- Assist in development and updates of SOPs and training materials
- Participate in audits, inspections, and regulatory reviews
- Act as liaison between regional teams, distributors, and global stakeholders
- Monitor updates in vigilance regulations and support compliance implementation
This role is critical in ensuring medical device safety, regulatory compliance, and effective risk management across global markets.
Eligibility / Qualifications
Educational Qualification:
Bachelor’s degree in Life Sciences, Clinical Sciences, Engineering, or related field
Relevant courses include:
B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Clinical Research, Biotechnology, Microbiology, Biochemistry, Biomedical Engineering, Clinical Data Management, Regulatory Affairs, Pharmacovigilance
Experience:
- 3 to 6 years of experience in pharmacovigilance, medical device vigilance, or post-market surveillance
Preferred Qualifications:
- Postgraduate certification in Pharmacovigilance, Medical Device Vigilance, or Regulatory Affairs
- Experience with ophthalmic or medical device products
- Exposure to global regulatory authorities and multi-market environments
Skills Required:
- Strong knowledge of vigilance systems and regulatory compliance
- Experience in complaint handling and safety reporting
- Excellent communication and stakeholder management skills
- Ability to work with global cross-functional teams
- High attention to detail and documentation accuracy
- Strong analytical and problem-solving abilities
Location & Salary
- Job Location: Ahmedabad, India
- Job Type: Permanent Full-Time
- Department: Regulatory Affairs / Pharmacovigilance
- Salary: Competitive salary package with additional employee benefits
Rayner offers a comprehensive benefits package including health and wellness programs, employee assistance support, and global recognition platforms.
Application Process
Interested candidates can apply directly through the official career portal:
Apply Here: https://careers.rayner.com/job/vigilance-specialist-india-5841510
Ensure your resume highlights experience in pharmacovigilance, complaint handling, regulatory reporting, and global safety systems.
Why Join Rayner?
- Work with a globally trusted medical device company
- Contribute to patient safety and healthcare innovation
- Exposure to global pharmacovigilance and regulatory systems
- Strong career growth in drug safety and regulatory affairs
- Opportunity to work with international teams and stakeholders
- Competitive salary and employee benefits
This role is ideal for professionals aiming to advance in pharmacovigilance, medical device safety, and global regulatory compliance.
Frequently Asked Questions (FAQs)
1. What experience is required for this role?
Candidates need 3–6 years of experience in pharmacovigilance or medical device vigilance.
2. Is medical device experience mandatory?
It is preferred but not mandatory. Pharmacovigilance experience is also acceptable.
3. What qualifications are required?
A degree in life sciences, clinical sciences, or engineering is required.
4. What is the job location?
The role is based in Ahmedabad, India.
5. What type of work will I handle?
You will manage complaint handling, safety reporting, regulatory submissions, and vigilance compliance activities.
Summary Table
| Category | Details |
|---|---|
| Company | Rayner |
| Vacancies | Vigilance Specialist |
| Required Education | B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Clinical Research, Biotechnology, Microbiology, Biochemistry, Biomedical Engineering, Regulatory Affairs, Pharmacovigilance |
| Experience | 3–6 Years in Pharmacovigilance / Medical Device Vigilance |
To apply for this job please visit careers.rayner.com.
