Strict Screening: Only candidates meeting the exact qualification and experience criteria listed below will be allowed to clear the initial screening and proceed to the technical interview rounds.
- Required Qualifications: Full-Time B.Pharm / M.Pharm / M.Sc Chemistry / M.Sc Analytical Chemistry only.
- Industry Type: Mandatorily from regulated pharmaceutical formulation manufacturing plants (USFDA / MHRA approved sites preferred).
- Shift Flexibility: Must be willing to work in all rotational shifts.
Positions Open for Walk-In:
1. Officer / Sr. Officer Wet Analysis (RM & PM)
- Experience Required: 2 to 5 Years
- Core Responsibilities:
- Perform routine physical, chemical, and wet chemistry testing on incoming Raw Materials (APIs/Excipients) and Packaging Materials.
- Execute manual/automated titrations, limit tests, assays, and moisture determination (Karl Fischer).
- Operate and calibrate laboratory instruments including FTIR, UV-Vis Spectrophotometers, and Autotitrators.
- Maintain error-free, real-time raw data logs adhering strictly to Good Documentation Practices (GDP) and GLP.
2. Officer / Executive – Stability Analysis
- Experience Required: 2 to 7 Years
- Core Responsibilities:
- Perform physical, chemical, and instrumental analysis of stability samples at designated time intervals.
- Strong hands-on proficiency in operating, running sequences, and basic troubleshooting of HPLC, GC, and Dissolution apparatus.
- Track stability chamber pull schedules and ensure strict data integrity (ALCOA+ principles) across software networks.
- Assist in identifying data trends and supporting laboratory investigations for Out of Trend (OOT) and OOS results.
3. Officer – Analytical Method Validation (AMV)
- Experience Required: 2 to 4 Years
- Core Responsibilities:
- Execute high-precision physical, chemical, and instrumental analysis dedicated to Method Validation, Method Verification, and Method Transfer (MV/MT).
- Run advanced analytical sequences on HPLC, GC, UV, IR, and Dissolution setups.
- Assist in compiling raw testing data to prepare high-quality validation protocols, transfer logs, and technical reports.
- Coordinate with internal team leads to flag parameters, discrepancies, or software anomalies observed during method validations.
Time and Venue
22nd October , 10.00 AM – 4.00 PM
Rubicon Research Limited.A-17, Phase II, Special Economic Zone (SEZ), Pithampur, District Dhar, Madhya Pradesh 454775