Ritsa Pharma
Website:
ritsapharma.com
Job details:
Experience: 2–7 Years
Key Responsibilities:
Perform routine analysis using analytical instruments such as HPLC (Fast LC), UV Spectrophotometer, and Dissolution Apparatus.
Conduct wet analysis including titrations, assays, and related chemical testing.
Work in a GxP-compliant environment, adhering to Quality Management System (QMS) requirements.
Ensure compliance with Good Documentation Practices (GDP) while recording and reporting data.
Prepare and maintain analytical reports, logs, and documentation accurately.
Follow Standard Operating Procedures (SOPs) and regulatory guidelines.
Support investigations related to OOS (Out of Specification) and deviations.
Perform instrument calibration and maintenance as required.
Coordinate with QA and production teams for quality-related activities.
Required Skills & Qualifications:
Bachelor’s/Master’s degree in Pharmacy, Chemistry, or Life Sciences (B.Pharm / M.Sc / B.Sc).
Strong hands-on experience in HPLC (Fast LC), UV, and Dissolution testing.
Knowledge of wet chemistry techniques.
Good understanding of GxP and QMS processes.
Familiarity with Good Documentation Practices (GDP).
Attention to detail and strong analytical skills.
Preferred Skills:
Experience in regulated pharmaceutical environment.
Exposure to audit and compliance activities.
Ability to handle multiple tasks and meet deadlines.
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