Take on a pivotal role as Analyst II in QA Validation, contributing to continuous improvement and compliance within a pharmaceutical context. This position suits candidates adept in validation methodologies and report writing.
As an Analyst II, you'll engage with the Validation team to write and execute essential validation protocols and reports. Your responsibilities will also include analysis of statistical data, technical support, and ensuring close communication with manufacturing. A commitment to cGMP practices and detail-oriented work will be vital in this role.
Key Responsibilities:
• Write and execute IQ, OQ, PQ validation protocols
• Analyze data for validation criteria compliance
• Conduct mapping studies using advanced monitoring devices
• Develop and update standard operating procedures
• Investigate and resolve deviations in validation studies
Requirements:
• Degree or diploma with relevant experience
• Minimum of 2 years in pharmaceutical env...