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    Rubicon Hiring BPharma & MPharma Candidates for Research Officer Role, Apply Online

    New Pharma Job opportunity 2026 | Rubicon Research is Hiring for an Officer role or Analytical method validation | Apply Now

    Looking for an Officer Job in the pharmaceutical industry? This exciting Pharma Job opportunity at Rubicon Research Limited offers professionals a chance to work in Analytical Method Validation at its Pithampur facility, Indore. Candidates with experience in analytical instruments and GMP-regulated environments can advance their careers through this excellent Officer Job in a leading pharma organization.

    • Job Title: Officer
    • Location: Pithampur, Indore, Madhya Pradesh, India

    About the Company

    Rubicon Research Limited is a pioneering research-driven pharmaceutical company, dedicated to delivering innovative and effective healthcare solutions. We specialize in novel formulations, with a strong focus on research and development, creating a significant impact on healthcare outcomes globally.

    Key Responsibilities

    • To perform physical and chemical, instrumental analysis of method validation/method verification & method transfer.
    • The candidate should have experience in HPLC, GC, UV, IR, and Dissolution testing.
    • Responsible for the preparation of protocols and reports for method validation/method verification.
    • Responsible for coordinating with the Analytical development team members in case of discrepancies observed during validation/verification/transfer.
    • To perform instrument calibration and working standard qualification.
    • If required, need to provide support for QC analysis as and when required.
    • Responsible for adherence to GLP and the Health, Safety, and Environment system in the laboratory.
    • To perform the task assigned by the supervisor/HOD as and when required.
    • Should have good written and communication skills.

    Qualifications

    • Bachelor’s / Master’s Degree in Science / Pharma.
    • The candidate should have experience in HPLC / GC / UV / IR / KF / Dissolution, etc.
    • He should have exposure to QC working under GLP, GDP, and GMP environments.
    • The candidate having experience in a US-FDA-approved company is more preferable.
    • Knowledge of Empower software will be an added advantage.
    • Should have the skill to achieve a deliverable task with minimal support for analysis.

    Additional Notes

    • The 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 for ensuring compliance with GLP, Health, Safety, and Environment requirements.

    CLICK HERE FOR ORIGINAL NOTIFICATION

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