Pharma Jobs in Mumbai: Advanz Pharma is Hiring a Senior Manager, Patient Safety | Apply Now
Are you currently looking for Pharma Jobs in Mumbai? ADVANZ PHARMA is hiring a Senior Manager, Patient Safety at its Mumbai office. This hybrid role offers an opportunity to contribute to the development, safety, and compliance of specialty, hospital, and rare disease medicines worldwide. The position calls for an experienced professional passionate about improving patient outcomes and maintaining the highest global standards in safety documentation and pharmacovigilance.
Job Details:
- Job Title: Senior Manager, Patient Safety
- Location: Andheri (East), Mumbai – Hybrid
About the Role:
The Senior Manager, Patient Safety will manage all aspects of Reference Safety Documents such as CCDS, SmPC, PI, PIL, datasheets, and product monographs for ADVANZ PHARMA products worldwide. The role ensures compliance with global and regional regulatory requirements and supports continuous improvement in safety documentation.
About ADVANZ PHARMA:
ADVANZ PHARMA is a global specialty pharmaceutical company dedicated to improving patients’ lives by providing and enhancing access to specialty, hospital, and rare disease medicines. Headquartered in London, UK, with a strong presence across Europe, Canada, Australia, and India, the company partners with innovative biopharma developers to bring essential treatments to patients worldwide.
ADVANZ PHARMA’s diverse product portfolio spans multiple therapeutic areas — including hepatology, gastroenterology, anti-infectives, endocrinology, critical care, and rare diseases. Its Centre of Excellence in Mumbai plays a key role in supporting global operations. The company is driven by its core values of Entrepreneurship, Speed, and Integrity, fostering a collaborative culture where innovation, inclusivity, and continuous learning are at the forefront.
ADVANZ PHARMA promotes diversity and gender equality, with nearly 40% of managers being women, and offers a dynamic, growth-oriented work environment where employees are empowered to take ownership, think creatively, and make a difference in global healthcare.
Education:
Postgraduate in Life Sciences or Pharmacy.
Key Responsibilities:
- Serve as a subject matter expert in global labeling and safety documentation.
- Manage safety-related variations, product information updates, and stakeholder communication.
- Oversee revision and approval of scientific documents, including SmPCs and PILs.
- Respond to Health Authority queries with scientific accuracy.
- Plan and coordinate global labeling compliance to meet regulatory standards.
- Ensure documentation aligns with Good Documentation Practices (GDP).
- Collaborate with teams across Patient Safety, Regulatory Affairs, and Medical Affairs.
- Maintain compliance with Pharmacovigilance Safety Master File (PSMF).
- Lead improvements in safety document management and SOP development.
- Stay updated with evolving pharmacovigilance (PV) regulations globally.
- Foster collaboration, accountability, and innovation aligned with company values — Entrepreneurship, Speed, and Integrity.
Skills:
- Strong experience in patient safety and reference safety document management (CCDS, SmPC, PI, PIL).
- Exposure to innovator molecules, generics, or biosimilars.
- Skilled in labeling systems like Veeva Vault and knowledge of EU QRD templates.
- Demonstrated leadership, collaboration, and communication abilities.
- Strategic, detail-oriented, and adaptable to global work environments.
How to Apply?
To apply, simply submit your updated CV and a cover letter detailing your experience and motivation to join our team.
