Job Description

We are looking for a

QA Executive

with hands-on experience in

Validation & Qualification

activities in a pharmaceutical manufacturing environment. The candidate should have strong knowledge of GMP requirements and regulatory guidelines and be capable of handling validation documentation and compliance activities independently.

Key Responsibilities:

Plan, execute, and review

Validation & Qualification

activities (DQ, IQ, OQ, PQ). Preparation, review, and approval of validation protocols and reports for equipment, utilities, systems, and processes. Handle

cleaning validation

, process validation, and re-validation activities. Ensure compliance with

cGMP, Schedule M, WHO, and regulatory guidelines

. Coordinate with production, engineering, QC, and other departments during validation activities. Review change controls, deviations, CAPA, and risk assessments related to validation. Support internal and external audits and regulatory inspections. Maintain proper documentation and records as per QA requirements.

Required Qualifications:

B.Pharm / M.Pharm / M.Sc (or equivalent qualification). 2-5 years of relevant experience in QA Validation & Qualification in a pharma company. Strong understanding of GMP, validation lifecycle, and regulatory compliance. Good documentation, analytical, and communication skills.

Preferred Skills:

Exposure to audits and regulatory inspections. Knowledge of HVAC, water systems, and computerized system validation (CSV) is an added advantage. Ability to work independently and as part of a cross-functional team.

Interested candidates can send their CV to:

hrd@fidopharma.com OR 9876115903

Job Type: Permanent

Pay: ?20,000.00 - ?40,000.00 per month

Benefits:

Health insurance Provident Fund
Work Location: In person