Real instrument time
Analysts run HPLC, GC and dissolution themselves from month one — not after a two-year queue.
RIVANOVA
Careers
We hire for rigour and curiosity, then give people the instruments, mentorship and autonomy to do the best work of their careers.
Why RIVANOVA
Pharmaceutical careers are built on hands-on time with real instruments and real batches. We hire fewer people than our size would suggest, and give each of them more.
Analysts run HPLC, GC and dissolution themselves from month one — not after a two-year queue.
Every new joiner is paired with a senior in their function for a structured first year.
Anyone can raise a quality concern directly to QA or the board, without going through a line manager.
Regulatory affairs, Six Sigma and analytical certifications are funded and given study leave.
Medical insurance covering employee, spouse, children and dependent parents.
Published rosters four weeks ahead, with overtime paid rather than absorbed.
Cross-functional moves are supported — several of our QA leads started in production.
A 12-month rotation across production, QC, QA and regulatory for B.Pharm, M.Pharm and M.Sc. graduates.
Current openings
Apply through the form below or email your CV to admin@rivanovahealthcare.com quoting the role reference.
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HPLC and GC analysis of raw materials, in-process samples and finished goods against pharmacopoeial monographs. B.Pharm or M.Sc. Analytical Chemistry.
Batch record review, deviation and CAPA management, change control and audit-trail review prior to release. Prior WHO-GMP site experience essential.
Granulation, compression and coating operations with in-process control responsibility. Experience with rapid mixer granulators and auto-coaters preferred.
Aseptic filling operations in Grade A/B environments, media fill participation and environmental monitoring coordination. Aseptic qualification required.
Pre-formulation, prototype development and scale-up for oral solid dosage forms. M.Pharm with demonstrated experience in modified-release systems.
CTD and ACTD dossier compilation, response to regulatory queries and lifecycle maintenance of export registrations across emerging markets.
Distributor appointment and management, field-force supervision and territory performance across Maharashtra and Gujarat.
A structured 12-month rotation across production, quality control, quality assurance and regulatory affairs. Open to B.Pharm, M.Pharm and M.Sc. graduates.
Application
Complete the form and email your CV to admin@rivanovahealthcare.com quoting the role reference. We acknowledge every application within three working days.