Rubicon Research Walk-In – Quality Control Formulations

Rubicon Research Walk-In Interview 2026 – Quality Control Formulations

Rubicon Research is recruiting experienced pharmaceutical professionals for Quality Control (QC) formulation jobs at its facility in Pithampur, Dhar, Madhya Pradesh. The walk-in recruitment covers Wet Analysis (Raw Materials and Packaging Materials), Stability Analysis, and Analytical Method Validation (AMV). Candidates with full-time B.Pharm., M.Pharm., M.Sc. Chemistry, or M.Sc. Analytical Chemistry qualifications and relevant pharmaceutical formulation manufacturing experience are eligible to apply. The advertised experience requirements range from 2 to 7 years, depending on the position.

Company Overview

Rubicon Research is a pharmaceutical formulations company focused on regulated markets. The advertised recruitment drive is for Quality Control professionals with experience in pharmaceutical formulation manufacturing.

Job Details

Current Job Openings

1. Officer / Senior Officer – Wet Analysis (RM & PM)

Experience: 2–5 years

Key Responsibilities:

• Perform physical, chemical, and wet chemistry testing of incoming raw materials, including APIs and excipients, and packaging materials.

• Conduct manual and automated titrations, limit tests, assays, and moisture determination using Karl Fischer methods.

• Operate and calibrate laboratory instruments, including FTIR, UV-Visible spectrophotometers, and autotitrators.

• Maintain accurate, real-time raw data records in compliance with Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).

2. Officer / Executive – Stability Analysis

Experience: 2–7 years

Key Responsibilities:

• Perform physical, chemical, and instrumental analysis of stability samples at scheduled intervals.

• Operate HPLC, GC, and dissolution apparatus, including sequence execution and basic troubleshooting.

• Track stability chamber sample-pull schedules and maintain data integrity according to ALCOA+ principles.

• Assist with data trend identification and laboratory investigations involving Out of Trend (OOT) and Out of Specification (OOS) results.

3. Officer – Analytical Method Validation (AMV)

Experience: 2–4 years

Key Responsibilities:

• Perform physical, chemical, and instrumental analysis for method validation, method verification, and method transfer activities.

• Execute analytical sequences using HPLC, GC, UV, IR, and dissolution equipment.

• Compile raw analytical data and assist in preparing validation protocols, transfer logs, and technical reports.

• Coordinate with team leads to identify discrepancies, parameters, and software anomalies during validation activities.

Eligibility & Qualifications

Candidates must meet the strict screening criteria specified in the recruitment advertisement.

• Required qualifications: Full-time B.Pharm., M.Pharm., M.Sc. Chemistry, or M.Sc. Analytical Chemistry.

• Industry experience: Experience in regulated pharmaceutical formulation manufacturing plants is mandatory.

• Preferred exposure: Candidates from USFDA- or MHRA-approved manufacturing sites are preferred.

• Shift requirements: Applicants must be willing to work all rotational shifts.

Only candidates meeting the specified qualification and experience requirements will be considered for the initial screening and technical interview rounds.

Walk-In Interview Details

How to Apply

Eligible candidates should attend the walk-in interview at the specified venue on 22 October 2026, between 10:00 AM and 4:00 PM.

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Job Summary