Quality Control Analyst

Ritsa Pharma; Hyderabad; On-site; INR 600,000 - 900,000; Full time

Job summary

Ritsa Pharma is seeking a laboratory professional to perform routine and non-routine analyses of raw materials, in-process samples, finished products, and stability samples. You will operate, calibrate, and troubleshoot analytical instruments such as HPLC, UV, IR, and GC, while ensuring GMP, GLP, and data integrity requirements are met.

Maintaining ALCOA+ lab documentation and supporting internal audits and CAPA initiatives will be part of your responsibilities, along with coordination with

Qualifications

• Hands-on experience with analytical instruments (HPLC, UV, IR, GC).
• Experience with GMP compliance and data integrity practices (ALCOA/ALCOA+).
• Familiarity with audits and regulatory expectations.

Responsibilities

• Perform routine and non-routine analysis of materials and samples.
• Operate, calibrate, and troubleshoot analytical instruments (HPLC, UV, IR, GC).
• Prepare and review analytical documentation, SOPs, COAs, and test reports.
• Ensure GMP, GLP and data integrity compliance; maintain ALCOA+ documentation.

Skills

HPLC

UV

IR

GC

GMP compliance

ALCOA/ALCOA+ data integrity

Tools

HPLC

UV

IR

GC

Job description

Technical Expertise

• Hands-on experience with HPLC, UV, IR, GC instruments
• Strong understanding of GMP compliance
• Knowledge and adherence to Data Integrity principles (ALCOA/ALCOA+)

Audits Faced

• Involved in facing regulatory and internal audits such as:
• USFDA / MHRA / WHO / GMP / ISO (mention whichever apply for the candidate)
• Supported audit preparedness, documentation, and CAPA implementation

Roles & Responsibilities

• Performing routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples.
• Operation, calibration, and troubleshooting of analytical instruments (HPLC, UV, IR, GC)
• Preparation and review of analytical documents, SOPs, COAs, and test reports.
• Ensuring compliance with GMP, GLP, and data integrity requirements.
• Maintaining lab documentation as per ALCOA+ principles.
• Handling OOS, OOT, deviations, and supporting investigations.
• Participating in internal and external audits; ensuring audit readiness.
• Maintaining good housekeeping, safety, and adherence to laboratory practices.
• Coordination with cross-functional teams to ensure timely release of batches and samples