Life Science Jobs: Advanz Pharma is Hiring a Senior Executive | Apply Now
Looking for Regulatory Affairs jobs to take your career to the next level? ADVANZ PHARMA, a global leader in specialty and rare disease medicines, is inviting talented Life Science professionals to join as Senior Executive – Regulatory Affairs (EU) in Mumbai. This life science job is your chance to work with an international pharmaceutical company known for innovation, integrity, and speed while shaping the future of healthcare!
Job Details:
- Job Title: Senior Executive – Regulatory Affairs (EU)
- Location: Andheri (East), Mumbai, India (Hybrid work model)
- Type: Temporary (8 months)
About the Company:
ADVANZ PHARMA is a leading global pharmaceutical company dedicated to improving patients’ lives through high-quality specialty, hospital, and rare disease medicines. Headquartered in London, UK, the company operates across 20+ countries including Europe, the US, Canada, Australia, and India.
With its Centre of Excellence in Mumbai, ADVANZ PHARMA is recognized for its entrepreneurial culture, collaborative environment, and strong commitment to quality and compliance. The company’s diverse product portfolio spans gastroenterology, hepatology, endocrinology, CNS, and critical care, making it a preferred destination for Life Science graduates aiming to excel in Regulatory Affairs Jobs.
Educational Requirements:
- Graduate or Postgraduate in Life Sciences or any science discipline.
- Formal training or certification in Regulatory Affairs is preferred.
Key Responsibilities:
- Prepare, review, and submit renewal and maintenance applications for Marketing Authorizations (MAs).
- Ensure all regulatory documentation meets EU Health Authority standards.
- Manage regulatory submissions (CTD Module 1 & 3) and variation applications.
- Collaborate cross-functionally to ensure timely supply continuity and product compliance.
- Provide peer review support and manage post-approval activities.
- Drive continuous improvement initiatives and ensure adherence to internal SOPs.
- Support readiness for health authority inspections and audits.
Skills Required:
- Strong knowledge of ICH & EU regulatory guidelines.
- Expertise in CTD Module 1 & 3 documentation and lifecycle management.
- Excellent project management and communication skills.
- Ability to work in a fast-paced, cross-functional environment.
- Positive attitude with problem-solving and decision-making capabilities.
- Demonstrated commitment to entrepreneurship, speed, and integrity – the core values of Advanz Pharma.
If you’re a passionate Life Science professional seeking to make a real impact in global healthcare, this is your chance to join ADVANZ PHARMA — a company that values innovation, collaboration, and patient-centric excellence. Don’t miss this opportunity to enhance your career in Regulatory Affairs Jobs with one of the most respected pharmaceutical brands in the world.
