Lyrus was built on a simple thesis: the pharma industry doesn’t need another CRO or another CDMO – it needs an integrated CRDMO that owns the whole arc from molecule to market. One team accountable for the science, the dossier and the supply agreement.
That model is designed to reduce hand-off risk and keep formulation, CMC and target-market requirements aligned. It supports customers in 50+ countries, including one ANDA that received first-cycle approval in approximately eight months in December 2023.
From taste-masked paediatric products to platform-enabled lifecycle extensions, we build products that stand out in crowded categories – with the IP position, the reviewer-ready dossier and the cGMP supply to back them up.
In 2016, C.P. Bothra, who had co-founded and led Medreich for over three decades, launched Lyrus with a sharper thesis than any of his previous companies: a science-first R&D house that owns the whole arc – from proprietary delivery science to reviewer-ready dossiers to global cGMP supply – under a single accountable team. What the family group built in fifty years of contract manufacturing and lifecycle brand-building for Cipla, SmithKline Beecham and Wyeth is the operating muscle Lyrus inherits from day one. What Lyrus adds is proprietary formulation IP – six drug-delivery technologies and a 16-granted / 74-filed patent portfolio – the moat the previous generations of the group never had.
DATE AND TIME:
- Date: Saturday, 14 November 2026
- Time: 10:00 AM to 4:00 PM
- Venue: Lyrus Life Sciences Pvt. Ltd, Research & Development Centre, No. 54A & 54B, Hoskote Industrial Area, Bengaluru 562122
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Contact Info:
- HR: Anjoo 7045040403 | Raju 6362008534 | Shivaling 7411872337
- careers@lyruslife.com
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JOB DETAILS:
- Formulation R&D (9 roles): 5 roles for 2–4 years’ experience and 4 roles for 4–10 years. You’ll need an M. Pharm in Pharmaceutics or Industrial Pharmacy and hands-on work with OSD, liquid oral and topical dosage forms, including scale-up and QbD for EU and US markets.
- Analytical R&D (10 roles): 3–8 years’ experience and an M.Pharm in Pharmaceutical Chemistry or an MSc in Chemistry. You should have done method development, validation and stability work on HPLC, GC, Malvern and dissolution.
- Regulatory Affairs (5 roles): 4–6 years’ experience and an M.Pharm. You’ll need experience with dossier compilation, eCTD submissions and query responses for EU, UK, TGA and RoW markets.
- Business Development (5 roles): 4–10 years’ experience and an M.Pharm, M.Tech or MBA. You should have handled client proposals, out-licensing and co-development deals across the UK, EU, MENA, SEA, LATAM and RoW.
Pay will match industry standards and depend on your experience and how the interview goes.
Please bring:
your updated resume,
your last three months’ salary slips,
your educational certificates,
your Aadhaar or PAN card.
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