Use Your Power for Purpose

Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need. 

What You Will Achieve

In this role, you will:

• Manage time effectively to meet targets and develop plans for team-based work activities, contributing to the completion of complex projects.

• Develop and validate manufacturing processes for drug products, ensuring compliance and data integrity.

• Create and review cGMP documentation, including batch records, cleaning assessments, and SOPs.

• Support manufacturing by troubleshooting investigations and implementing Corrective Action/Preventative Action to prevent issues.

• Provide expertise in operations for new lines and processes directly associated with.

• Lead environmental tasks, initiatives, training, and services in compliance with Pfizer Global Environment, Health & Safety Standards, and regulatory requirements.

• Offer subject matter expert input during regulatory inspections.

• Use judgment to modify methods and techniques as needed.

How You Will Achieve It

The Sr. Production Supervisor will:

• Supervise colleague work activities in production of Drug Products in compliance with Good Manufacturing Practices (GMP's) as well as all federal, state, and local environmental and safety regulations.

• Actively engage in colleague development, including timely performance feedback/appraisals as well as through other aspects of the performance management process (i.e. 1:1s, IDPs).

• Ensure colleague training is maintained and in compliance with appropriate procedures, specifications and standards.

• Schedules staffing, optimizing labor available to meet required product demands of customers within budgeted guidelines, communicating with and recommending actions to leadership as needed.

• Collaborates cross-functionally with Quality, Maintenance, Warehouse and other production personnel to ensure information is properly shared and production remains on schedule.

• Completes operational quality, environmental, and safety incident investigations as required.

• Identifies process improvements and supports continuous improvement initiatives related to compliance, safety and production to minimize risk, ensure product quality and reduce waste through the application of OpEx and IMEX principles.

• Reviews batch records, supports release of production lots and ensures product meets quality and quantity standards.

• Maintains and improves labor standards as it relates to having the proper number of colleagues assigned to each line per the line standards to meet staffing and financial guidelines.

• Champions a safety culture by aiding in the establishment of safety rules and instruction. Adheres to safety requirements. Reports events to EH&S. Ensures events are contained and appropriate steps are taken to mitigate risk to product and the manufacturing environment.

• Assists manager with special projects and other duties as assigned or needed.

Here Is What You Need (Minimum Requirements)

• High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience

• Strong understanding of cGMP and regulatory requirements

• Proficiency in troubleshooting and problem-solving within a manufacturing environment

• Excellent communication and organizational skills

• Ability to work independently and as part of a team

• Experience with process validation and documentation

• Familiarity with environmental, health, and safety standards

Bonus Points If You Have (Preferred Requirements)

• Experience in a pharmaceutical manufacturing environment

• Knowledge of Lean Manufacturing principles

• Proficiency in data analysis and statistical tools

• Strong project management skills

• Ability to mentor and train junior colleagues

• Experience with regulatory inspections and audits

• Strong attention to detail and commitment to quality

• Ability to adapt to changing priorities