Neovantt is hiring talented Research Associates in Analytical Development (2–4 years) with strong expertise in HPLC, dissolution testing, method development, validation, and experience in injectable analytical method development.
This role is ideal for candidates passionate about pharma analytical R&D, ICH/USP/EU guidelines, and advanced analytical instrumentation. If you’re looking to grow in a high-performance R&D environment, this opportunity is for you.
Key Responsibilities
- Perform analysis of raw materials, finished products, and stability samples.
- Conduct analytical method development for in-process, intermediate, and final product testing.
- Work with advanced instruments:
- HPLC, LCMS, GC, UV, Microscope, Osmometer
- Dissolution Apparatus (Type I–IV)
- Karl Fischer (KF) and Malvern Particle Sizer
- Handle working standards, reference standards, primary standards, and vendor samples.
- Conduct method verification, validation, protocol preparation & report writing.
- Follow GLP, sample handling SOPs, and documentation practices.
- Apply ICH, USP, and EU guidelines for analytical method development for OSD, injectables, NCEs, and 505(b)(2) products.
- Perform any additional tasks assigned by seniors or HOD.
Eligibility & Qualifications
- PG Degree:
- M.Sc. (Organic/Analytical Chemistry)
- M.S./M.Pharm (Any Specialization)
- Experience: 2 to 4 years in Analytical Development Laboratory (ADL)
- Preference for candidates with Injectable Method Development experience.
Why Join Neovantt?
- Work with advanced analytical technologies.
- Exposure to regulatory-driven analytical development.
- Career growth in formulation & analytical R&D.
- Opportunity to contribute to global quality standards.
How to Apply
Eligible candidates may email their updated CV to:
📩 hr@neovantt.com
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