Role & responsibilities

Strict Screening: Only candidates meeting the exact qualification and experience criteria listed below will be allowed to transparent 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 Positive Documentation Practices (GDP) and GLP.
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.
Solid 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.
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.

📌 Walk Interview For Officer / Executive Quality Control Formulation Pithampur
🏢 Rubicon Research
📍 Pithampur