Pharmacovigilance & Regulatory Affairs Lead

Boots; Greater London, Nottingham; On-site; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Boots Retirement Savings Plan

Discretionary annual bonus

Enhanced parental leave

Job summary

Boots is seeking a Safety Advisor to join our Quality & Technical Services team. You will maintain vigilance processes across pharmacovigilance, medical device vigilance and cosmetovigilance, ensuring compliance with regulatory standards and internal policies.

Collaboration with customers, healthcare professionals and regulators will be key to successful post‑market surveillance. You will review safety data, prepare reports, and contribute to PSURs and trend analysis, while supporting audits,

Qualifications

• Experience reviewing safety data in a regulated environment.
• Strong attention to detail and regulatory compliance.
• Ability to manage multiple priorities and meet regulatory timelines.

Responsibilities

• Maintain pharmacovigilance, medical device vigilance, and cosmetovigilance processes.
• Liaise with customers, healthcare professionals, regulators, and internal stakeholders for post-market surveillance.
• Review, evaluate, and document safety reports and other product safety information.
• Analyze safety data to support case processing, trend analysis and escalation of concerns.
• Contribute to PSMF sections, procedures, signal management, literature reviews and PSURs.
• Manage cosmetovigilance activities and cosmetic product safety programs.

Skills

Product safety

Regulatory compliance

Post-market surveillance

Data review

Education

Science degree

Tools

Drug safety databases

Job description

Boots is seeking a Safety Advisor to join our Quality & Technical Services team. You will maintain vigilance processes across pharmacovigilance, medical device vigilance and cosmetovigilance, ensuring compliance with regulatory standards and internal policies.

Collaboration with customers, healthcare professionals and regulators will be key to successful post‑market surveillance. You will review safety data, prepare reports, and contribute to PSURs and trend analysis, while supporting audits,