Bausch + Lomb has listed a career opportunity in Pharmacovigilance and Medical Affairs for experienced professionals in India. The position focuses on pharmacovigilance vendor oversight, individual case safety report (ICSR) quality review, medical device safety reporting, and post-marketing surveillance activities.
This opportunity may suit candidates with a pharmacy, nursing, or related educational background and experience in pharmacovigilance, materiovigilance, or post-marketing surveillance. The role involves reviewing adverse event reports, ensuring regulatory compliance, coordinating with external vendors, and supporting local safety reporting requirements.
According to the supplied job description, candidates should have at least three years of relevant experience in the pharmaceutical or medical environment. The position is associated with Mumbai, India, although the detailed job description also references Gurgaon, so applicants should confirm the exact work location before applying.
Bausch + Lomb Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Bausch + Lomb |
| Job Title | Pharmacovigilance Specialist |
| Functional Area | Global Pharmacovigilance and Risk Management / Medical Affairs |
| Job Location | Mumbai, India, according to the listing header |
| Location Mentioned in Detailed Description | Gurgaon, India |
| Qualification | Bachelor’s, Master’s, or Doctorate degree in Pharmacy, Nursing, or a related discipline |
| Experience Required | Minimum 3 years |
| Relevant Experience | Pharmacovigilance, Materiovigilance, or Post-Marketing Surveillance |
| Key Responsibilities | ICSR quality review, vendor oversight, safety reporting, regulatory compliance |
| Employment Type | Not specified in the supplied details |
| Salary | Not disclosed |
| Job Posting Date | October 26, 2026 |
| Application Mode | Online through the official careers portal |
About Bausch + Lomb
Bausch + Lomb is a global eye health company with a portfolio of products serving a wide range of vision and eye care needs. The company works across research, development, manufacturing, and commercial activities in the eye health sector.
Its pharmacovigilance and risk management functions help monitor product safety, review adverse event information, and support compliance with applicable regulatory reporting requirements.
Job Description: Pharmacovigilance Specialist
The Pharmacovigilance Specialist will support vendor oversight and safety case quality activities for pharmaceutical products and medical devices. The role requires reviewing individual case safety reports, monitoring vendor performance, ensuring timely reporting, and maintaining compliance with local and global pharmacovigilance procedures.
The position also covers post-marketing surveillance, medical device safety reporting, medical affairs support, SOP management, employee training, and readiness for audits and regulatory inspections.
The detailed job description refers to the business title Vendor QC Associate, Pharmacovigilance and Materiovigilance – Medical Affairs, India, while the listing headline uses Pharmacovigilance Specialist. Candidates should verify the exact title on the official application page.
Key Responsibilities
1. Pharmacovigilance Vendor Oversight and Quality Review
- Monitor the quality and compliance of case processing performed by external vendors.
- Review vendor procedures and working instructions to ensure they remain complete and up to date.
- Analyse weekly and monthly case quality data to identify improvement and training needs.
- Review adverse event (AE), serious adverse event (SAE), and medical device event reports.
- Clarify medical issues, raise queries, verify case assessments, and improve case narratives.
- Review MedDRA terminology and coordinate with vendors and internal medical personnel.
- Implement improvements to case processing quality and operational efficiency.
2. Drug Safety Reporting
- Support local pharmacovigilance activities and the responsibilities assigned to the company’s local PV designee.
- Receive, document, and process adverse event reports from spontaneous reports, literature, and other sources.
- Handle medication error and pregnancy-related safety cases.
- Support data entry into global safety databases, follow-up activities, and record archiving.
- Coordinate expedited reporting of individual case safety reports to the relevant local regulatory authority.
- Review applicable pharmacovigilance sections of data exchange agreements.
- Help manage pharmacovigilance agreements with third-party distributors.
3. Post-Marketing Surveillance
- Support post-marketing surveillance programmes and re-examination activities for new drugs, where applicable.
- Coordinate with Regulatory Affairs, Medical Affairs, and Clinical Operations.
- Oversee contract research organisation (CRO) activities according to study protocols, SOPs, and regulatory requirements.
- Prepare or review study documents, including protocols, case report forms (CRFs), periodic reports, and final re-examination applications.
- Support local regulatory submissions.
- Coordinate the reporting of serious adverse events to CDSCO India and the global safety function.
4. Medical Device Safety Reporting
- Receive and document adverse events associated with medical devices.
- Enter relevant information into the global safety database.
- Coordinate follow-up activities and maintain case records.
- Prepare and submit adverse event and safety information reports within applicable regulatory timelines.
- Maintain appropriate documentation and archiving records.
5. Medical Affairs Support
- Support Medical and Scientific Affairs activities across products and business units.
- Assist with the review of promotional materials for marketed products.
- Provide medical information to internal and external customers within approved product labelling.
- Support suitability assessments and tier evaluations for healthcare professional speakers.
- Coordinate with key opinion leaders (KOLs) on posters, abstracts, publications, and other scientific outputs.
- Assist with medical education programmes related to relevant treatment areas and products.
6. SOP Development and Training
- Develop and update local SOPs covering pharmacovigilance, post-marketing surveillance, and safety information management.
- Support updates to global and regional vigilance procedures and work instructions.
- Provide training and guidance on drug safety reporting to relevant employees, vendor support staff, and third-party distributors.
- Help ensure that personnel understand applicable reporting responsibilities and procedures.
7. Audits, Inspections, and CAPA
- Support pharmacovigilance audits and regulatory inspections.
- Maintain audit-ready documentation and coordinate inspection-related activities.
- Work with compliance teams on non-conformances and deviations.
- Assist with preparing corrective and preventive action (CAPA) documentation.
- Support improvements to vendor oversight and case processing compliance.
8. Documentation and Record Management
- Maintain internal and external correspondence related to assigned responsibilities.
- Archive pharmacovigilance, vigilance, and post-marketing surveillance records according to company procedures.
- Ensure documentation follows applicable local regulatory requirements.
- Perform other vigilance-related duties as assigned.
Eligibility Criteria
Educational Qualification
Candidates should have a degree in one of the following areas or a related discipline:
- Pharmacy
- Nursing
- A related scientific or healthcare discipline
The supplied description accepts a Bachelor’s, Master’s, or Doctorate degree from an accredited college or university.
Work Experience
Applicants should have a minimum of three years of experience in one or more of the following areas:
- Pharmacovigilance
- Materiovigilance
- Post-Marketing Surveillance
Experience in individual case safety report review or medical device event review is preferred.
Required Skills
Candidates should demonstrate the following knowledge and abilities:
- Understanding of global pharmacovigilance and materiovigilance regulations.
- Knowledge of post-marketing surveillance requirements.
- Experience reviewing individual case safety reports or device event cases.
- Familiarity with safety databases; LSMV and CatsWeb are mentioned as preferred systems.
- Knowledge of medical terminology and general medicine or pharmacy.
- Strong written and verbal communication.
- Excellent interpersonal and teamwork skills.
- Attention to detail and effective work prioritisation.
- Organisation, strategic planning, and project management capabilities.
- Ability to coordinate with vendors, internal departments, and external stakeholders.
Job Location
The listing header identifies Mumbai, India, while the detailed job description states Gurgaon, India.
Because these locations do not match, candidates should confirm the actual work location and any office attendance requirements through the official Bausch + Lomb careers portal before applying.
Salary and Benefits
The salary for this position has not been disclosed in the supplied India vacancy details.
The compensation paragraph included in the supplied description refers to US-based employment and contains placeholder salary figures. It should not be treated as the salary range or benefits package for this Indian position.
Candidates should check the official vacancy page or contact the employer for India-specific compensation, insurance, leave, and other employment benefits.
How to Apply for Bausch + Lomb Recruitment 2026
Interested candidates should apply through the official Bausch + Lomb careers website.
Application steps:
- Visit the company’s official website.
- Navigate to the Careers section.
- Search for “Pharmacovigilance Specialist” or the detailed title “Vendor QC Associate, Pharmacovigilance and Materiovigilance – Medical Affairs, India”.
- Verify the location and experience requirements.
- Submit your updated resume through the official recruitment portal.
The link above leads to the company’s website, not a verified direct application link for this specific vacancy. Use the official careers section to locate the relevant opening.
Frequently Asked Questions (FAQs)
1. What position is Bausch + Lomb hiring for?
The supplied listing advertises a Pharmacovigilance Specialist position. The detailed job description uses the business title Vendor QC Associate, Pharmacovigilance and Materiovigilance – Medical Affairs, India.
2. Where is the job located?
The listing header specifies Mumbai, India, while the detailed description mentions Gurgaon. Candidates should confirm the correct location with the employer.
3. What is the minimum experience required?
The job description specifies at least three years of experience in pharmacovigilance, materiovigilance, or post-marketing surveillance.
4. What qualifications are accepted?
A Bachelor’s, Master’s, or Doctorate degree in Pharmacy, Nursing, or a related discipline is mentioned.
5. What are the main responsibilities?
The role includes vendor oversight, ICSR quality review, drug and medical device safety reporting, post-marketing surveillance, SOP management, training, and audit support.
6. Is medical device safety experience relevant?
Yes. The description includes medical device adverse event reporting and materiovigilance activities.
7. Which safety databases are preferred?
LSMV and CatsWeb are mentioned as preferred systems in the supplied job description.
8. What is the salary for this position?
The India-specific salary has not been disclosed in the supplied vacancy details.
9. How can I apply?
Candidates should visit the official Bausch + Lomb website and use its Careers section to locate the relevant vacancy.
10. What is the application deadline?
The supplied job description does not specify an application deadline. Candidates should check the official careers portal for the current status.
Disclaimer
This article is based on the supplied Bausch + Lomb job description dated October 26, 2026. The listing title and detailed business title differ, and the location information references both Mumbai and Gurgaon. Candidates should confirm the exact role, work location, current vacancy status, salary, and application instructions through the official recruitment portal before applying.