• Plan, review, and execute qualification and validation activities, including equipment, utilities, facilities, processes, cleaning, and computerized systems.

• Prepare and review validation protocols, reports, risk assessments, and related documentation.

• Ensure validation activities comply with cGMP, regulatory guidelines, and approved procedures.

• Review validation deviations, investigations, and CAPAs and ensure timely closure.

• Coordinate with Production, Engineering, QC, IT, and other functions to ensure effective execution of validation activities.

• Support regulatory and internal audits related to validation and qualification.

• Monitor validation status and ensure timely completion of the validation plan.

• Provide technical guidance to junior team members and support continuous improvement initiatives.

Requirements

• Bachelor's degree in Pharmacy, Science or a related field.

• 4–7 years of relevant experience in QA Validation/Qualification within the pharmaceutical industry.

• Strong knowledge of GMP and validation principles.

• Hands-on experience in equipment, process, cleaning, utilities, and/or computerized system validation.

• Good knowledge of risk assessment and validation documentation.

• Strong analytical, problem-solving, communication, and organizational skills.

• Good command of English.