Supervisor Of Validation, Calibration & Qualification (Qa Departement)

Supervisor of Validation, Calibration & Qualification will oversee the development, implementation, and maintenance of the validation, calibration, and qualification programs for all equipment, facilities, and systems in the pharmaceutical manufacturing process. The Supervisor will ensure that all validation, calibration, and qualification activities are performed in accordance with cGMP regulations, internal policies, and procedures.

Responsibilities

• Develop and maintain a comprehensive validation, calibration, and qualification program for equipment, facilities, and systems used in the pharmaceutical manufacturing process

• Ensure that all validation, calibration, and qualification activities are performed in accordance with cGMP regulations, internal policies, and procedures

• Develop and maintain standard operating procedures (SOPs) for validation, calibration, and qualification activities

(etc)

Qualifications

• Pharmacist

• At least 5 years of experience in validation, calibration, and qualification in a pharmaceutical manufacturing environment

• Strong knowledge of cGMP regulations, FDA guidelines, and industry best practices related to validation, calibration, and qualification

• Experience in managing a team of validation, calibration, and qualification specialists