Help us build India's next-generation pharmaceutical CDMO.
Biodeal Pharmaceuticals is a high-growth Pharmaceutical CDMO backed by Piramal Alternatives and expanding across injectable manufacturing, nasal spray CDMO, nutraceuticals and international export markets. We're building a world-class manufacturing team — and we're looking for talented, purpose-driven professionals who want to make a genuine impact in global healthcare.
Six reasons to build your career here.
A rare combination of regulated-market credentials, frontier specialisations and institutional backing.
World-class certifications
Work at one of India's few WHO-GMP and PIC/S certified CDMOs — the credentials that open regulated export markets.
Nasal spray frontier
Be part of India's leading Nasal Spray CDMO team — a frontier specialisation in intranasal drug delivery.
Injectable growth
Contribute to a high-growth sterile injectable operation backed by institutional investment.
DSIR R&D environment
Develop novel formulations across pharmaceuticals, nutraceuticals and intranasal delivery in a government-recognised R&D centre.
Global footprint
A 56-country export reach, with ambitions to enter the US, EU and Australian regulated markets.
Institutional backing
A ₹110 Crore Piramal Alternatives investment — financial stability and a clear growth trajectory.
Current openings.
Explore each role, and apply directly below. Don't see your fit? Send a speculative application and we'll keep you on file.
Join our DSIR-approved R&D centre to design and optimise new formulations across pharmaceuticals, nasal sprays and nutraceuticals — from first prototype to a robust, scalable commercial formula.
What you'll do
- Design and develop new formulations across dosage forms
- Run lab-scale trials and ICH stability studies
- Support scale-up and technology transfer to manufacturing
- Maintain development documentation to regulatory standards
What we're looking for
- B.Pharm / M.Pharm or equivalent
- 2+ years in formulation development
- Exposure to orals, nasal or injectable dosage forms (a plus)
- Strong analytical and documentation skills
Own quality-assurance activities across our sterile injectable operation at Paonta Sahib — ensuring every batch meets WHO-GMP and Schedule M standards.
What you'll do
- Review batch records and in-process controls
- Manage deviations, CAPA and change control
- Support internal audits and regulatory inspections
- Help maintain the quality management system
What we're looking for
- B.Pharm / M.Sc
- 2+ years QA in sterile / injectable manufacturing
- Working knowledge of WHO-GMP and Schedule M
- Meticulous documentation and attention to detail
Prepare and manage CTD / ACTD dossiers and product registrations for Indian and international markets — helping take our products into regulated destinations.
What you'll do
- Compile and maintain CTD / ACTD dossiers
- Manage product registrations and renewals
- Liaise with regulatory authorities and partners
- Track evolving regulatory requirements across markets
What we're looking for
- B.Pharm / M.Pharm
- 1–3 years in regulatory affairs
- Exposure to export-market filings (a plus)
- Excellent written communication
Run day-to-day production on our nasal spray lines — overseeing filling, sealing and in-process controls in validated clean rooms.
What you'll do
- Supervise nasal spray manufacturing operations
- Ensure GMP compliance on the shop floor
- Maintain batch records and in-process checks
- Coordinate with QA, engineering and maintenance
What we're looking for
- B.Pharm / Diploma in Pharmacy
- 2+ years in pharmaceutical production
- Nasal spray or liquid-filling experience (a plus)
- Hands-on, process-driven mindset
Positions are managed via our CMS and refreshed as new roles open.
Submit your application.
Share your details and attach your resume — our team reviews every application and responds to shortlisted candidates within two weeks.
Don't see the right role?
We're always keen to hear from exceptional people. Send a speculative application and tell us where you'd make an impact.