Senior Production Operator; SPO

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them.

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.

Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run.

Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations.

Perform in-process quality inspections, and seek to implement process and safety improvements.

High School Diploma or GED with 2+ years of relevant experience

Strong analytical and problem-solving skills

Excellent problem-solving and decision-making skills

Excellent communication and interpersonal skills

Ability to work independently and as part of a team

Detail-oriented with strong organizational skills

Previous experience in cGMPs (current Good Manufacturing Practices) environment

Proficiency in using manufacturing software and tools

Ability to adapt to changing priorities and work in a fast-paced environment

Demonstrated leadership skills and ability to mentor team members

Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

Stand 8-12 hours per shift, sit 2-4 hours per shift, use computer terminal 1 hour per shift.

Change into area required garments (i.e. scrubs, shoes, PPE, safety glasses) 2-3 times per shift.

Work around moving/rotating equipment, work around chemicals, work in hearing conservation area, work on knees or non-standing position occasionally for repairs. Requires physical activity for equipment repair, adjustment and operation of equipment.

Respond to visual/audible warning and alarm indicators, respond to color or other visual indicators.

Walk on floors/catwalks, climb stairs/ladders

Must be able to lift up to 50 pounds.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

12 hour night shift, rotating weekly. Overtime as needed.

OTHER JOB DETAILS

Last Date to Apply for Job:
March 11th, 2026

Eligible for Relocation Package: NO