QO Technical Associate II; 1st Shift

Overview

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.

In this role, you will:

• Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.
• Manage personal time and professional development, being accountable for results.
• Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.
• Identify and solve moderately routine problems.
• Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.
• Ensure work is reviewed for accuracy, quality, and adherence to standards.
• Evaluate and interpret data for accuracy, precision, and trends, considering the impact on cGMP and recommending corrective actions when necessary.
• Operate efficiently in a fast-paced, customer-oriented team environment, analyzing raw materials and packaging samples to support the company's quality program in the chemistry lab.
• Complete training activities, maintain records, equipment, basic lab supplies, and reagents in compliance with Current Good Manufacturing Practices (GxP).
• Participate in laboratory investigations and Quality Performance Reviews.

• High School Diploma or GED with 2+ years of relevant experience
• Basic math and computer skills such as data entry
• Understanding of equipment, instrumentation, and computer applications
• High productivity and the ability to multi-task
• Ability to read, comprehend, and follow procedures
• Good oral, written, and interpersonal communication skills within a diverse team setting
• Experience in a GMP environment

• Quality Control experience
• Strong problem-solving and analytical skills
• Ability to work independently with moderate supervision
• Previous laboratory experience, including a basic understanding of microbiology and aseptic technique.

• Laboratory and office work requiring walking, standing, and sitting throughout a shift.
• Long periods of standing and working in glove ports/half-suit of an isolator may be needed.
• Occasional lifting (less than 25 kg) and reaching may be required.
• Extended time working at a computer

Schedule is on 1st shift, typically Monday - Friday 8 hour shift. This position requires colleagues to work weekends and/or holidays to meet business or customer needs. All Laboratory colleagues adhere to safe work practices such as wearing appropriate personal protective equipment including lab coat, safety glasses, and gloves. There is no routine travel associated with this position.

Last Date to Apply for Job: 3/19/26

Work Location Assignment:
On Premise

The salary for this position ranges from $20.07 to $33.45 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 to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.

Learn more at Pfizer Candidate Site – U.S. Benefits. Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Michigan - Kalamazoo location. Relocation assistance may be available based on business needs and/or…