POSITION SUMMARY

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.

EDUCATION

• Diploma in Science (preferably related to Chemistry) or Chemical Process Technology.
• Degree in Science (preferably related to Chemistry) or Chemical Process Technology.

EXPERIENCE

A minimum of 1 year QC experience in an analytical laboratory is preferred.
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control

(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

Job Related Requirements

• Effective problem-solving skills.
• Demonstrated ability to perform in a team.
• Knowledge of cGMPs and ALCOA principles

POSITION RESPONSIBILITIES

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.

Job Related Requirements

• 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

Supervisor, the key responsibilities are:

• Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOP