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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