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 setting. 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
• Strong 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.
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