Why KMS
Work that follows the product.
One programme, end to end
You work alongside formulation, analytical, transfer and regulatory colleagues on the same product, not in a silo.
Products that reach regulated markets
Programmes developed here have been approved by regulators including the US FDA, the UK MHRA and Health Canada.
Learn from experienced leads
Scientific leads with decades in pharmaceutical development mentor the teams they run.
Teams
Where you could work.
Formulation development
Oral solids, oral liquids, ointments and topical semisolids, and sterile products, from preformulation to pilot scale.
Analytical development
Method development and validation, impurity profiling, nitrosamines, elemental impurities, IVRT and stability.
Technology transfer
Scale-up, exhibit batches and site-to-site transfer with manufacturing partners.
Regulatory affairs
Dossier compilation and filing for the US, EU and rest-of-world markets.
Quality assurance
GLP, data integrity, instrument qualification and audit readiness across the laboratories.
Project management
Keeping partner programmes on scope, budget and timeline, from agreement to delivery.
Open roles
There are no roles listed right now.
We still read every application, and keep strong profiles on file for upcoming vacancies.
Apply
Send us your application.
Fill in the details below and your email app will open with the application addressed to Human Resources. Attach your CV (PDF, DOC or DOCX) and send.
Start a conversation
Where does your programme stand?
Tell us the molecule, the dosage form and the market you are filing in. A programme lead will read it and reply with what we would do next.
Business enquiries: vasanthi@kmshc.com · +91 97898 75194V-23