Rubicon Research Pvt Ltd extends an invitation for walk-in interviews for various positions within the Quality Control department on October 22, 2026. The company seeks candidates with full-time qualifications in B.Pharm, M.Pharm, M.Sc in Chemistry, or M.Sc in Analytical Chemistry, specifically from regulated pharmaceutical formulation manufacturing environments, preferably those approved by USFDA or MHRA. Applicants must demonstrate flexibility to work across all rotational shifts. The available roles include Officer/Sr. Officer for Wet Analysis, requiring 2 to 5 years of experience. Another position is for Officer/Executive in Stability Analysis, which demands 2 to 7 years experience. Lastly, the Officer role in Analytical Method Validation (AMV) calls for 2 to 4 years of experience.
Department: Quality Contro
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.
Open Positions
Officer / Sr. Officer Wet Analysis (RM & PM)
- Experience: 2 to 5 Years
- 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.
Officer / Executive – Stability Analysis
- Experience : 2 to 7 Years
- 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.
Officer – Analytical Method Validation (AMV)
- Experience: 2 to 4 Years
- 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-in interview details
Date of interview: 22nd October 2026
Timings: 10.00 AM – 4.00 PM
Venue: Rubicon Research Limited.A-17, Phase II, Special Economic Zone (SEZ), Pithampur, District Dhar, Madhya Pradesh – 454775.
About Rubicon Research Pvt Ltd
Rubicon Research Pvt. Ltd., now Rubicon Research Limited, is a Mumbai-based, R&D-driven pharmaceutical formulations company founded in 1999. Started as a contract formulation development provider, the company operationalized its oral-solids manufacturing facility at Ambernath, Maharashtra in 2011 and since 2012 has focused on developing, manufacturing and commercializing its own branded specialty and generic prescription products, predominantly for the highly regulated US market. With its principal R&D centre in Thane, India and a development centre for inhalation and nasal products in Ontario, Canada, and two USFDA-inspected, cGMP-compliant manufacturing facilities in Maharashtra, Rubicon has a portfolio of 55+ commercialized products in the US across 69 active NDAs and ANDAs – including oral capsules, tablets, liquids, suspensions and syrups, ophthalmic drops, delayed and extended-release tablets, and drug-device combinations like nasal sprays.