QC ​​IM Lab Analyst III​

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) Applicant must have HS Diploma or GED and 8 years of relevant experience; OR and Associate's degree with 6 years of experience; OR an Bachelor's degree (preferably in Chemistry or other related Science) with 4 years of relevant 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 Incoming Material inspection experience with components. AQL Inspection; Defect Recognition 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      PHYSICAL/MENTAL REQUIREMENTS Stand up for up to 8 hours, sit for up to 8 hours, walking, climbing stairs, responding to visual warning indicators, respond to audible warning indicators, respond to color or special visual indicators, wear specialized protective clothing (lab coat, safety glasses, gloves, face shield/goggles, apron), repetitive use of upper extremities. May have to lift objects approximately 10 pounds. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS There are no out of the ordinary travel or shift requirements associated with the position.   Individual will be expected to work nonstandard schedule as needed to support the business objectives Work Location Assignment: On Premise OTHER JOB DETAILS Last Date to Apply for Job August 28th, 2026 
The salary for this position ranges from $25.88 to $43.14 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and