QC Chemist Testing

Description

• Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
• Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
• Assist / troubleshoot laboratory technical problems.
• Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
• Use Imex "way of working" for day-to-day operations, problem solving, escalation and continuous improvements.
• Perform / review and document analytical testing (In-Process, Raw Materials, API samples) and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.
• Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
• Support laboratory investigations and perform equipment troubleshooting where required.
• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
• Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).
• Set up and maintain QC processes (e.g. reference standards and retention sample management), perform investigations as required for any associated deviations.
• Conduct training for fellow colleagues from QC and other departments (e.g. Production).
• Uphold Pfizer's code of conduct and values.
• Collaborate with cross-functional teams to drive flawless execution.
• Play an active and impactful role in Tier processes by updating performance against metrics, highlighting issues, with appropriate escalations. Support development and implementation of solutions.
• Contribute to the continuous improvement activities in QC laboratory or cross functional teams as nominated.
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Qualifications

• Effective problem-solving skills.
• Demonstrated ability to perform in a team.
• Knowledge of cGMPs and ALCOA principles.
• Possess a can-do / pride to succeed attitude.
• Embrace the use of digital technology to scale and speed up every form of interaction and action.
• Degree in Science (Chemistry)
• A minimum of 1 year QC experience in an analytical laboratory is preferred.