Candidates should possess experience working with Laboratory Equipment and Calibration, including routine operation, preventive maintenance, and instrument calibration checks.
Perform systematic trend analysis of audit, self-inspection, and regulatory observations, identifying recurring issues, compliance risks, and continuous improvement opportunities within the QMS, and provide actionable recommendations to functional owners and senior management
To develop and revise the quality assurance framework for the company and to modify and improve the existing production standards and Standard Operating Procedures (SOPs), when necessary.
· To develop and revise the quality assurance framework for the company and to modify and improve the existing production standards and Standard Operating Procedures (SOPs), when necessary.
To develop and revise the quality assurance framework for the company and to modify and improve the existing production standards and Standard Operating Procedures (SOPs), when necessary.
Review and approve GMP documents, including SOPs, protocols, reports, and change controls, to ensure compliance with Pfizer global and local documents.
Ensure payment reminder messages, Promise to Pay (PTP), Early Collection Activities (ECA) and Letter of Demand (LOD) communications are accurate and appropriate.
Review Method Statements (MOS) and Material Submissions (MES) to ensure they comply with project specifications, client requirements, and applicable codes and standards.