At Parexel, we all share the same goal – to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special – a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.
At Parexel, your expertise shapes patient-focused progress. 💚
We’re inviting experienced professionals to our Walk-In Drive for opportunities in Regulatory Intelligence and Regulatory Affiliate roles.
📅 Walk-In Drive Details:
- Walk in Drive : 20th December, 2025,
- Time: 10am Onwards
- Venue: Arliga Ecoworld, Building No. 5B, 3rd
floor, Sarjapur Marathali, Outer Rind
Road, Devarabeesanahalli Village,
Varthur, Hobli, Bangalore East Taluk,
Bengaluru – 560103
Open Roles:
– Regulatory Intelligence Specialist
– Regulatory Affiliate Specialist
(Experience: 2–6 years)
Key Skills We’re Looking For:
✔ Regulatory Intelligence: Staying updated on evolving local and regional regulatory requirements, interpreting guidelines, and communicating insights to global and local teams; participating in regulatory forums, meetings, and conferences to share best practices and strengthen organizational knowledge.
✔ Regulatory Affiliate: Reviewing and submitting dossiers, negotiating with Health Authorities for approvals, and collaborating with local Regulatory, Medical, Marketing, and Market Access teams to support and assess the impact of regulatory changes.
Join a team where expertise meets purpose.
Check the complete Job description before joining the drive or apply below: https://lnkd.in/g7NH59G9
Open Roles:
– Regulatory Affairs Consultant
– Senior Regulatory Affairs Associate
– Regulatory Affairs Associate
(Experience: 2–10 years)
Key Skills We’re Looking For:
✔ Experience in Biologics: lifecycle management, renewals, biologics/vaccines/monoclonal antibodies, and global submissions (US, EU, Japan, Canada, Switzerland, Australia)
✔ Labelling expertise: country-specific regulations, CCDS/USPI, SPL, packaging components, and post-approval updates
✔ Strong understanding of global regulatory frameworks and CMC requirements
You can explore the full job descriptions through (the link) before joining the drive or apply below
Come be part of a team that works With Heart. ❤
https://lnkd.in/gQhMeW4h
https://lnkd.in/g4Nyywgk
https://lnkd.in/gD5nE9eB
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