Senior Executive

Rubicon Research Limited; Indore District; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Rubicon Research Limited is seeking a Sr. Executive (Reviewer/Investigator) for its Quality Control department in Pithampur. The role involves reviewing analytical data, ensuring GLP adherence, and handling OOS and deviations with a focus on timely material release.

The candidate should have 6–12 years of experience in analytical chemistry, with proficiency in HPLC/GC/UV and other instrumental analyses. Willingness to work in shifts and travel to plant locations as needed.

Qualifications

• Degree in Science or Pharmacy required (BSc/ MSc).
• Experience with analytical data review and GLP practices.
• Familiarity with instrumental analysis (HPLC/GC/UV/IC/IR/KF/Dissolution).
• Knowledge of Chromeleon software is an added advantage.

Responsibilities

• Prepare and review specifications, SOPs, protocols, and reports.
• Handle incidences, OOS, Change Control, Deviations and CAPA.
• Coordinate with external labs for material release within timelines.
• Ensure availability of reagents, columns, standards, instruments, and documents.
• Adhere to GLP, Health, Safety and Environment requirements.

Skills

Analytical data review

GLP compliance

Communication skills

Education

Bachelors / Masters in Science or Pharma

Tools

HPLC

GC

UV

IC

IR

KF

Dissolution

Chromeleon 7.2

Job description

Job Description

Position / Job Title - Sr. Executive (Reviewer/Investigator)

Department - Quality Control

Reporting To - Assistant Manager (P3) / Manager (P4).

Location - Pithampur

Years of Experience - 6 to 12 years

Dosage Form - Solid Oral

Job Responsibilities / Deliverables

• Preparation and review of Specification, SOPs, Protocols, Reports, summary sheets, water samples report etc. To review analytical raw data of LNB / AWR for compliance, correctness and completeness.
• To handle and ensure completion of all incidences, OOS, Change Control, Deviations etc.
• To coordinate with external testing laboratory for the release of material within the time frame assigned.
• To ensure resources (Chemicals / Reagents / Analytical columns / Standards / Documents / Instruments / Equipment’s etc.) available to smooth line function whenever required.
• To perform the task assigned by the supervisor/HOD as and when required.
• Responsible to adherence of GLP and Health, Safety Environment system in Laboratory.
• Should have good written and communication skill.

Qualifications & Pre-Requisites

• Bachelor / Master Degree of Science / Pharma.
• He should have good experience of analytical data review and good knowledge of Chemical analysis, instrumental analysis like HPLC/GC/UV/ IC/IR/KF/Dissolution.
• He should have experience of Handling and ensuring completion of all incidences, OOS, Change Control, Deviations etc. Responsible for ensuring completion of GLP activities.
• The candidate having experience in US-FDA/MHRA approved company is preferable.
• Knowledge of Chromeleon 7.2 software will be an added advantage.
• Should have skill to achieve deliverable task with minimum support for analysis.

Additional Notes

• Role is expected to work in all shifts.
• If required, the candidate should be ready to travel to all plant locations on work priority as per company policy.
• Responsible to ensure compliance to GLP, Health, Safety and Environment requirement.