Senior Associate QA (24/7 Shift)

• Perform all activities in compliance with safety standards and SOPs.
• Write, review and approve Standard Operating Procedures in accordance with Policies.
• Provide Quality support for triage and investigation of all classes of non-conformance (NC) events.
• Review and approval of deviations for closure ensuring compliance with appropriate documentation.
• Participates in customer complaint investigations.
• Provides training and advice to staff in order for them to perform their desired functions.
• Observe and provide real-time quality oversight, and support for production unit operations, extending to formulation, vial and Syringe Fill Finish related activities, including observation and provision of direction during media fills and assessment of aseptic interventions.
• Review/approve production batch records, and associated documentation in preparation for Qualified Person disposition activities.
• Review and approve cGMP records ensuring compliance with appropriate documentation.
• Support continuous improvement and Operational Excellence initiatives.
• Any other tasks/projects assigned as per manager’s request.

• University degree. Engineering or Science related discipline preferred.
• 4+ years’ experience working in the pharmaceutical or biotechnology industry
• Demonstrated ability in problem solving and experience in managing Root Cause Analysis /Deviation investigations

Life Science Recruitment