Become a key player as a QC Compliance Specialist with a renowned pharmaceutical company in Waterford. This hybrid role involves oversight in QC validation and documentation, balancing on-site and remote work.
This 23-month contract position focuses on ensuring regulatory compliance within validation activities. You will review protocols, manage deviations, and coordinate Change Control Requests while working collaboratively in a hybrid environment. Your expertise in Quality Control operations and laboratory settings will empower the company's commitment to quality assurance.
Key Responsibilities:
• Review and approve validation documentation promptly • Document deviations and manage corrective actions effectively • Raise and coordinate Change Control Requests accurately • Ensure compliance with FDA and EMA validation standards • Develop validation quality documents with precision
Requirements: • 2-5 years' experience in QC validation roles • Solid foundation in pharmaceutical quality control • Hands-on knowledge of QC equipment connectivity • Proficiency in validation documentation preparation • Familiarity with risk assessment methodologies
Apply your regulatory expertise and validation skills at this leading pharmaceutical company in Waterford. #J-18808-Ljbffr