Job Title

Become a specialist in validation processes at a leading pharmaceutical facility. Focus on documentation and protocols to ensure high-quality standards in compliance with Good Manufacturing Practices. As an Associate Validation Specialist, you will develop, execute, and modify validation documents critical to equipment and manufacturing processes. This role requires a collaborative approach to interact with multiple departments, ensuring the quality of products is consistently maintained. Knowledge of pharmaceutical practices and technical skills are essential for success in this impactful position. Key Responsibilities: Write validation protocols for equipment and processes Execute and document validation procedures accordingly Summarize reports and recommend corrective actions Participate in equipment selection from a validation perspective Train personnel on protocol execution requirements Requirements: Bachelor's degree in Natural Science or Engineering Minimum 2 years of pharmaceutical or technical experience Strong project management and communication skills Knowledge of Good Manufacturing Practices Innovative problem-solving abilities required Elevate quality assurance by ensuring compliance and validation in a fast-paced pharmaceutical environment. #J-18808-Ljbffr