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Inventia Healthcare Limited is conducting a walk-in interview for talented and experienced professionals in the Analytical R&D department. This is a great opportunity for candidates looking to build a career in method development and validation within a reputed pharmaceutical organization.
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Interview Date & Time
- Date: Saturday, 4th April 2026
- Time: 10:00 AM to 2:00 PM
Introduction
Inventia Healthcare Limited is known for its innovation-driven approach in drug delivery systems and pharmaceutical development. The company is inviting skilled candidates for Analytical R&D roles focusing on method development and validation.
Quick Details
- Role: Analytical R&D – Method Development & Method Validation
- Experience: 2–6 Years
- Qualification: M.Sc / M.Pharm
- Location: Thane West
Job Summary
The selected candidates will be responsible for analytical method development, validation, and handling advanced analytical instruments. The role requires hands-on experience in HPLC and GC along with a strong understanding of regulatory compliance and validation processes.
Job Criteria
- Experience in method validation for drug products and APIs
- Knowledge of method transfer and forced degradation studies
- Understanding of GLP/QMS compliance
- Hands-on experience with HPLC and GC
- Strong analytical method development expertise
- Knowledge of calibration, validation, and data interpretation
- In-depth understanding of validation processes and regulatory guidelines
- Candidates currently working in QC are not eligible
How to Apply
Interested candidates can directly attend the walk-in interview with the required documents.
Venue / Address
A 215, Inventia Healthcare Limited
Thane West – 400604
FAQ
Q1. Who can apply for this role?
Candidates with 2–6 years of experience in Analytical R&D with M.Sc or M.Pharm qualification can apply.
Q2. Is QC experience acceptable?
No, candidates currently working in QC are not eligible.
Q3. What documents should I carry?
Carry your updated CV and one passport-size photograph.
Q4. What skills are required?
Hands-on experience in HPLC, GC, method validation, and regulatory knowledge is required.
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