Sobre este puesto de Senior Production Operator (SPO) II en Pfizer
Use Your Power for Purpose
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members who understand the importance and impact of their role in Pfizer’s mission. You will help to ensure that patients and physicians have the medicines they need when they need them. The significance of your role cannot be overstated, as it directly influences the availability of essential medications. Your dedication and agility are crucial in maintaining the high standards of our manufacturing processes. By continuously striving for excellence, you contribute to the overall mission of delivering life-saving treatments to those in need. Your commitment to improving outcomes ensures that our breakthroughs reach the patients who depend on them.
What You Will Achieve
The Senior Production Operator II is responsible for the proper operation and maintenance of assigned production equipment. Performing routine preventative maintenance and repair of production equipment, and operation of the equipment during manufacturing.
Coach/trainer for others. SME for the process operations as it relates to the production equipment within respective area.
In this role, you will:
Self-motivated with ability to work in a team environment and independently.
Work in a clean manufacturing environment, requiring special garments to be worn. Demonstrated proficiency in gown/de-gown (i.e. aseptic) process.
Responsible for the proper operation of production equipment, equipment downtime, and scrap rate.
Perform machine set-up, repairs, adjustments, changeovers, emergency repair/replacement, and preventative maintenance on production equipment per the applicable procedures.
Interact and interpret data from production equipment automated control systems and displays.
Adhere to all safety requirements (e.g. PPE, LOTO, etc.) and process step requirements (e.g. SOP, Batch Records).
Communicate and inform management of all safety issues, quality issue, and equipment repair plan of action recommendations.
Communicate effectively with team members and management to achieve production deliverables and schedule adherence.
Support the Integrated Manufacturing Excellence (IMEx) activities (e.g. Continuous Improvement (CI), Standard Work (SW), and Total Productive Maintenance (TPM) including tracking metrics).
Demonstrated proficiency in current Good Manufacturing Practices (cGMP), Good Documentation Practice, and following detailed instructions.
Demonstrated proficiency working with automated production equipment.
Demonstrated proficiency in troubleshooting and Root Cause analysis.
Certified Trainer. Coaches and trains new hires.
SME of the production equipment within respective area.
Here Is What You Need (Minimum Requirements)
High School Diploma or GED
4+ years of experience
Proficiency in Good Manufacturing Practices (GMP) and related systems
Ability to troubleshoot and resolve technical issues
Strong organizational skills and attention to detail
Capability to work independently and as part of a team
Ability to adapt to changing priorities and manage multiple tasks
Ability to communicate effectively across departments and follow written and verbal instructions.
Bonus Points If You Have (Preferred Requirements)
Experience in pharmaceutical manufacturing or a related field
Knowledge of regulatory requirements and quality standards (cGMP)
Experience with Lean Manufacturing principles
Familiarity with Pfizer's Learning Solution and Quality Tracking System
Ability to train and mentor less-experienced colleagues
Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity
Work Environment & Operational Conditions
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 Requirements
24x7 operations with a rotating 12-hour shift schedule. Will work alternating weekends and holidays based on A/B shift schedule.
Typical start/end time:
6am to 6pm (day shift)
6pm to 6am (night shift)
Ability to work overtime as required.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
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.
Manufacturing