Use Your Power for Purpose

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

• Prepare Standard Operating Procedure (SOP) and Standard test procedures (STP) in accordance with actual practices, current GMP, and regulatory requirements, in QC Chemical Lab.
• Execute the project (i.e method validation/verification, etc.) in QC Chemical in the most effective way and meet the target date.
• Develop and/or perform method validation/ verification in accordance with the approved protocol and provide report.
• Support QC Supervisor to manage and maintain the implementation of compendia compliance in QC Chemical Lab.

Here Is What You Need (Minimum Requirements)

• BA/BS degree from Pharmaceutical Science or Chemical Science with any years of experience
• Solid understanding of common laboratory databases
• Familiarity with regulatory compliance requirements for pharmaceutical manufacturing
• Ability to work effectively both independently and as part of a team
• Proficiency in using quality system Standard Operating Procedures

Bonus Points If You Have (Preferred Requirements)

• Experience in a pharmaceutical chemical laboratory
• Strong problem-solving skills
• Ability to manage multiple tasks and projects simultaneously

  
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

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