Walk-in Interview for Quality Control (QC) & AQA - Formulations

About the Company

Shilpa Medicare Limited began as an API manufacturer in 1987 in Raichur, Karnataka, and started commercial production in November 1989. It has grown into a global supplier of affordable APIs and formulations across regulated markets.

Role Overview

This opening is for analytical services in Quality Control (QC) and Analytical Quality Assurance (AQA) for formulations. The position focuses on method validation, finished product analysis, review of analytical records, and compliance with GMP, data integrity, and regulatory expectations.

QC Responsibilities

• Carry out analytical method validation work and track validation parameters in line with ICH and ANVISA requirements.
• Prepare, examine, and maintain method validation protocols, raw data, and final validation reports.
• Perform analytical testing for finished dosage forms, including oral and injectable products, while meeting regulatory standards.
• Use laboratory instruments such as HPLC, GC, FTIR, UV-Visible spectrophotometer, and moisture determination tools like Karl Fischer.

AQA Responsibilities

• Check and approve analytical documents, raw data, audit trails, calibration and preventive maintenance records, analyst qualification files, and reference or working standard qualification documents.
• Monitor LIMS records, chromatographic systems, and stability chamber performance to ensure data accuracy, compliance, and quality expectations.

Candidate Profile

A male candidate is preferred for this role.

Eligibility

Applicants with any graduation background or a B.Pharma degree in any specialization may apply.

Perks and Benefits

No specific perks or benefits were mentioned in the source.

Additional Information

This is a walk-in opening based in Hyderabad, India.