QA Validation Officer
Major Duties and Responsibilities
• Ability to write technical protocols and reports with supervision in accordance with procedural requirements and current regulatory standards.
• Writes validation reports ensuring outcome of protocol objectives are documented.
• Supports execution of qualification and validation protocols
• Ensures validation is in accordance with the SVMP and Regulations
• Works in collaboration with other departments
• To communicate instantly any problems/queries to Senior Validation Officers/Validation Manager
• Identify issues and problems during validation, raising incident reports and timely closure.
• Identifies and reports quality events to the Validation Manager
• Revises standard operating procedures and WRKs in line with company policies and procedures.
• Supports delivery of key Quality Organisation Metrics in relation to Validation activities
• Ensures Validation Incident reports are raised.
• Ensues safety standards are met and maintained
• Undertakes such other reasonable duties as may be required from time to time to support the department and business activities
• Acknowledges responsibility to ensure an effective Quality Management System in order to achieve Quality Objectives
Competencies
• Responds promptly to requests and concerns
• Complete business objectives
• Ensure behaviors follow company policies and departmental expectations
• Team Work
• Problem Solving
• Effective Communication
• Customer Service
• Business Awareness
Knowledge and Experience
• Typical Years of Experience- 1-2 years experience
• Minimum Expected Education – Level 6 – Bachelor’s
• Additional Information -Degree University degree; typically, a minimum of 2 years experience working in a pharmaceutical GMP environment of which, at least 1 years’ experience is in pharmaceutical validation – preparing qualification documentation.
A minimum of two ‘A’ levels or T levels in a suitable discipline.