QC Chemical Raw Material Analyst

Use Your Power for Purpose

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our flexible, innovative, and customer-oriented quality culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve. Join us in our mission to improve patient outcomes through excellence in every aspect of our work.

What You Will Achieve

• Serve as a key resource and potentially lead lower-level team members within your area of expertise.
• Manage personal time and professional development, taking accountability for your results and prioritizing workflow.
• Contribute to project and departmental tasks, providing direction and training to team members, and may act as a lead worker.
• Be recognized as a "LEAD" or "Subject Matter Expert" in your field.
• Proactively identify and resolve basic complexity problems, considering wider implications.
• Complete assignments independently, selecting appropriate methods, and ensuring team assignments are completed.
• Review non-standard work for technical soundness and may review others' work.
• Adhere to Pfizer standards, guidelines, and values, influencing teams, and contributing to the development of departmental standards and guidelines.
• Provide input for performance assessments, ensure timely and compliant documentation, and develop processes to enhance cGMP standards.
• Maintain high standards of safety and housekeeping, participate in Continuous Improvement projects, and ensure adherence to all policies and procedures, while providing training and conducting peer reviews.

Here Is What You Need (Minimum Requirements)

• High School Diploma or GED
• 6+ years of experience
• Certifications in the relevant areas, if applicable
• Ability to write clear technical documents
• Good organizational and time management skills
• Proficiency in Microsoft Office
• Experience with laboratory equipment and procedures
• Knowledge of Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP)

Bonus Points If You Have (Preferred Requirements)

• Bachelor's Degree
• Pharmaceutical quality control and stability experience
• Effective problem-solving skills
• Strong analytical skills
• Strong attention to detail
• Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

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.

Global pharmaceutical company developing vaccines, oncology, and immunology treatments. Headquartered in New York, NY.

pfizer.com