QC Analyst

QC Analyst Our client is a leading pharmaceutical company committed to quality, innovation, and regulatory excellence.

Role Overview: The QC Analyst (Analytical Chemistry) plays a key role in ensuring the quality and compliance of manufacturing processes and products outputs through advanced chemical analysis and quality control activities. This position contributes directly to the organization’s commitment to product integrity, regulatory compliance, and continuous improvement by applying deep technical expertise within a GMP-regulated environment.

This is a 6-month contract role, with a 16/5 shift schedule and a shift premium.

• Independently execute advanced and complex chemical analyses to support quality control activities
• Ensure quality control processes comply with regulatory standards and internal quality systems
• Lead and support laboratory operations, including equipment qualification, routine maintenance, and troubleshooting
• Provide technical guidance, mentoring, and support to junior team members
• Drive continuous improvement initiatives to optimize laboratory processes, efficiency, and compliance
• Collaborate across departments to troubleshoot and resolve complex problems

• Manage quality control processes to ensure high standards of quality and regulatory compliance
• Ensure laboratory operations adhere to regulatory requirements, managing documentation and reporting effectively
• Maintain laboratory operations, including routine equipment maintenance and troubleshooting, to ensure smooth and efficient workflow
• Prepare detailed reports on quality control and manufacturing deviations, collaborating closely with Quality Assurance
• Ensure proper functioning of laboratory instruments and equipment by establishing routine maintenance and troubleshooting protocols
• Implement process improvements in quality control and laboratory operations to enhance efficiency and compliance
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• Maintain thorough and accurate documentation in compliance with regulatory standards

• Strong expertise in analytical chemistry with the ability to perform complex analyses independently
• Solid understanding of quality control systems and regulatory expectations (e.g., GMP)
• Advanced technical expertise to independently solve complex problems
• Experience preparing technical documentation, deviation reports, and investigation summaries
• Ability to provide technical guidance, share knowledge, and strengthen team capabilities
• Effective communication and collaboration skills across departments