Title:  Sr. Officer, Validation

Job Purpose
To perform day-to-day and routine validation activities to ensure that all challenges are resolved effectively and in a timely manner, in compliance with SOPs, GMP, and WHO requirements.

Responsibilities

• Follow all relevant quality instructions to ensure work is carried out in a controlled and consistent manner.

• Carry out the day-to-day operations related to the role to ensure continuity of work.

• Adhere to all relevant departmental policies, processes, standard operating procedures, and instructions so that work is performed in a consistent and compliant manner.

• Apply technical knowledge by following established procedures and/or standard practices to perform basic analyses.

• Prepare and review validation documents, systems, SOPs, protocols, reports, and their implementation.

• Prepare and review validation documents for pharmaceutical premises, utilities, and equipment, including systems, SOPs, protocols, reports, and implementation.

• Prepare and review validation documents for computerized systems, including systems, SOPs, protocols, reports, and implementation.

• Prepare and review process validation documents, including systems, SOPs, protocols, reports, and implementation.

• Prepare and review cleaning validation documents, including systems, SOPs, protocols, reports, and implementation.

• Prepare and review transportation validation documents, including systems, SOPs, protocols, reports, and implementation, in accordance with the latest requirements.

Qualifications, Experience & Skills

• Minimum Qualifications: Bachelor’s degree in Pharmaceutical Sciences or Science.

• Minimum Experience: 4 years