Senior QC Analyst

PFIZER ASIA MANUFACTURING PTE. LTD.; Singapore; On-site; SGD 45,000 - 65,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a Quality Control team member to perform analytical testing and ensure compliance with quality standards. You will be responsible for troubleshooting issues, authoring GMP documentation, and collaborating with cross-functional teams. A diploma in science and problem-solving skills are essential for success in this role. This position requires shift work and adherence to strict safety procedures.

Qualifications

• Able to work in shift (IPC team).
• Possess a can-do / pride to succeed attitude.
• Embrace the use of digital technology to enhance interactions.

Responsibilities

• Perform / review analytical testing accurately according to protocols.
• Assist in troubleshooting laboratory issues.
• Author GMP documentation as required.
• Collaborate with teams to enhance execution.

Skills

Effective problem solving skills

Ability to perform in a team

Knowledge of cGMPs and ALCOA principles

Education

Diploma in Science (related to Chemistry) or Chemical Process Technology

Job description

What You Will Achieve

The incumbent is a member of the Quality Control (QC) Laboratory team. Under the supervision of the QC Manager / Supervisor, the key responsibilities are:

• 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.
• Assist in troubleshooting laboratory technical problems and support laboratory investigations.
• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
• Use Imex "way of working" for day-to-day operations, problem solving, escalation and continuous improvements.

Responsibilities

• 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 support laboratory investigations as required.
• Assist in equipment troubleshooting where required.
• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
• Author GMP documentation (e.g. operational procedures) as required.
• 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.

Here Is What You Need (Minimum Requirements)

• Able to work in shift (IPC team)
• Diploma in Science (preferably related to Chemistry) or Chemical Process Technology.
• 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.

Bonus Points If You Have (Preferred Requirements)

• A minimum of 1 year QC experience in an analytical laboratory is preferred.

Work Location Assignment: On Premise