Perform internal audits of R&D and quality labs, ensure regulatory compliance, maintain laboratory equipment and reagents, verify/calibrate instruments, support chemical/physical analyses, manage SOP use and BMS alarms, and lead continuous improvement projects for Integrated Manufacturing Excellence in the Drug Product unit.
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:
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
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.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
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:
- Conduct internal audits of R&D and Quality laboratories to ensure readiness for regulatory agencies' audits.
- Ensure compliance with regulatory policies, procedures, and practices, identifying discrepancies in product safety and recommending corrective actions.
- Maintain laboratory area, equipment, and facilities in a clean, orderly, and operational state, ensuring availability and proper storage of reagents and reference standards.
- Perform verification or calibration of instruments and equipment, supporting chemical and physical analyses on samples for annual product review.
- Develop good working practices and guidelines for staff to use quality system Standard Operating Procedures, managing review and approval of Building Management System Alarms.
- Lead the Continuous Improvement (CI) process for Integrated Manufacturing Excellence (IMEx) within the Drug Product unit, identifying and conducting continual improvement projects.
Here Is What You Need (Minimum Requirements)
- BA/BS degree with any years of experience, or Associate's degree with 4+ years of experience, or high school diploma (or equivalent) with 6+ years of relevant 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 microbiology laboratory
- Strong problem-solving skills
- Ability to manage multiple tasks and projects simultaneously
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
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.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
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Top Skills:
ChatgptCmmsMicrosoft Copilot
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