Role & responsibilities

- Perform analytical method validation and method verification activities.

- Operate and troubleshoot analytical instruments such as HPLC and GC.

- Execute analytical testing as per approved protocols and SOPs.

- Prepare and maintain method validation reports and laboratory documentation.

- Ensure compliance with cGMP, GLP, and regulatory requirements.

- Coordinate with QC and other departments for validation-related activities.

- Maintain laboratory records and ensure data integrity.

Preferred candidate profile

- Hands-on experience in method validation.

- Practical knowledge of HPLC and GC instruments.

- Experience in the pharmaceutical formulation department is preferred.

- Positive understanding of cGMP, GLP, and analytical documentation.

- Strong analytical and troubleshooting skills.

- Must be willing to work at a pharmaceutical manufacturing plant.

Interested candidates please share the details to [email protected]

📌 Walk-in || QC-Method validation-Formulation (Hyderabad)
🏢 Reycruit
📍 Hyderabad