Senior Product Operator (SPO) II Carps VI-14

Posted 2 Hours Ago
Be an Early Applicant
McPherson, KS
Hybrid
Mid level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
The Senior Product Operator is responsible for operating and maintaining production equipment, ensuring compliance with safety and quality standards, troubleshooting issues, and training colleagues, all within a clean manufacturing environment.
Summary Generated by Built In

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

  • Take responsibility for individual contributions to achieve team deliverables, represent the work group within department teams, and foster a positive team environment.
  • Manage personal time and professional development, prioritize workflow, and assist less-experienced colleagues in prioritizing their tasks.
  • Complete assignments based on established procedures, identify delivery and process improvements, troubleshoot issues, and provide direction and training to team members.
  • Share knowledge within and across multiple work groups and deliver comprehensive technical training to colleagues.
  • Proactively identify and resolve non-routine problems, making decisions between multiple options in a structured environment.
  • Work under general supervision, complete recurring assignments independently, and refer new or unusual problems to the supervisor.
  • Ensure non-standard work is reviewed for sound technical judgment and hold oneself accountable to Pfizer standards, guidelines, and values.
  • Generate work orders, ensure tasks are completed accurately and promptly, and maintain compliance with safety guidelines and processing standards like cGMPs.
  • Adapt standard methods and procedures, identify necessary delivery and process improvements, and determine suitable methods for various work situations.
  • Maintain accurate records, monitor equipment usage, collaborate with supervisors on investigations and process improvements, and generate reports to assess training needs and track progress.


ROLE RESPONSIBILITIES

  • 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 work 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.


Basic Qualifications:

  • Applicant must have a Bachelor's degree with at least 2 years of experience; OR a Master's degree with more than 0 years of experience; OR an Associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience.
  • Problem solving mindset.
  • Possess necessary mechanical skills to perform the required machine set-up, repairs and adjustments in order to keep equipment operating efficiently.
  • Proficiently operate/maintain various standard maintenance tools/equipment including basic hand and power tools, multi-meters, and other mechanical equipment.
  • Ability to read, interpret, and perform job duties described in operating procedure, product batch records, and other equipment related documentation (e.g. vendor manuals, P&ID, schematics, drawings, etc.).


Preferred Qualifications:

  • 3+ years of relevant pharmaceutical manufacturing experience as operator/mechanic.
  • Technical school/ Auto Mechanic Program Certificate and/or Industrial maintenance/repair experience.


PHYSICAL/MENTAL REQUIREMENTS

  • 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

  • 24x5 operations with a rotating 12-hour shift schedule.
  • Typical start/end time:
  • 6am to 6pm (day shift)
  • Ability to work overtime as required.


No travel required.
OTHER JOB DETAILS
Last Date to Apply for Job: April 28th, 2025
The salary for this position ranges from $22.94 to $38.24 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 | (uscandidates.mypfizerbenefits.com). 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 - Kansas - Mcpherson location.
Relocation assistance may be available based on business needs and/or eligibility.
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.
Manufacturing
#LI-PFE

Top Skills

Automated Production Equipment
Cgmp
Good Documentation Practice
Maintenance Tools

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The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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