Senior Pharmaceutical Validation Engineer

About the Role

Our client is seeking a highly skilled Senior Pharmaceutical Validation Engineer to join their operations team based in Wolverhampton . This critical role ensures that all manufacturing processes, equipment, facilities, and utilities within the pharmaceutical manufacturing environment meet rigorous quality standards and regulatory compliance requirements. You will lead validation projects, develop validation strategies, and oversee execution to guarantee the integrity and safety of our products. This position offers a significant opportunity to impact product quality and compliance within a respected pharmaceutical manufacturing organization, contributing to the consistent delivery of safe and effective medicines.

Key Responsibilities

• Develop and execute validation master plans (VMPs) and detailed validation protocols for manufacturing processes, equipment, analytical methods, and cleaning procedures.
• Conduct validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Analyze validation data, prepare comprehensive validation reports, and manage deviations and change controls related to validation activities.
• Ensure all validation activities comply with current Good Manufacturing Practices (cGMP), FDA, EMA, and other relevant regulatory guidelines.
• Provide technical expertise and guidance to project teams, manufacturing personnel, and quality assurance on validation-related matters.
• Perform periodic reviews and revalidations to maintain the validated status of systems and processes.

Requirements

• Bachelor's degree in Engineering (Chemical, Mechanical, Electrical), Pharmacy, or a related scientific field.
• Minimum of 5 years of experience in validation engineering within the pharmaceutical or biotechnology industry.
• In-depth knowledge of validation principles, risk assessment techniques, and regulatory requirements (e.g., ICH Q7).
• Experience with process validation, equipment qualification, and computer system validation (CSV).
• Strong technical writing skills and the ability to interpret and apply complex technical documentation and regulatory standards.

Benefits

• Competitive salary and performance-based incentives.
• Hybrid working model offering flexibility between office and remote work.
• Comprehensive healthcare benefits package, including medical, dental, and vision.
• Generous paid time off and company holidays.
• Opportunities for career advancement and professional development within a growing company.