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Site production finite scheduler

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Pfizer

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Location:
United States , Sanford

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Category:

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Contract Type:
Not provided

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Salary:

82700.00 - 133900.00 USD / Year

Job Description:

Schedule and plan all manufacturing activities critical to monoclonal antibody or vaccine commercial operations. Deliver and maintain detailed process schedules that align the Plan of Record and Standard Work models to ensure the manufacture of product is carried out efficiently and in the correct sequence across the Media, Buffer, Upstream Suites, Downstream Suites and DP/DS Filling Areas. Utilize SAP and other MRP tools to enable production. Coordinate work orders and preventative maintenance with the associated organizations.

Job Responsibility:

  • Create and maintain the detailed process schedule for the assigned manufacturing area that aligns with the Plan of Record
  • Liaise with the production teams to create, maintain, and communicate the detailed production schedule
  • Maintain process orders from release to delivery/confirmation to ensure a high level of demand accuracy
  • Track actual production vs. plan and root cause for missed production opportunities (manufacturing attainment)
  • Collaborate in a cross functional team to ensure that activities that impact production (maintenance, changeover, etc.) are included in the schedule and planned to minimize production down time
  • Manage material movements (product intermediates) within the assigned manufacturing area
  • Collaborate with the Weigh and Dispense scheduler to ensure materials are available for production when needed
  • Collaborate with Production Planners and Material Planners to ensure schedule alignment raw material/component availability
  • Serve as a single point of contact representing Supply Chain for the area assigned

Requirements:

  • Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an Associate’s degree with 6 years of experience OR a Bachelor’s degree with at least 2 years of experience OR Master’s degree with more than 0 years of experience
  • Experience in a GMP environment in the biotech or pharma industry, preferably in manufacturing or supply chain
  • Proficient using SAP MRP
  • Ability to work independently and as part of a team
  • Excellent interpersonal skills
  • Good understanding of process manufacturing/ computer systems
  • Demonstrated ability to lead change and strong collaborative skills
  • Proactive and effective communication within and across shifts
  • Skilled using Microsoft Office, particularly Excel, Word, and PowerPoint

Nice to have:

  • Experience with technology transfer
  • Experience with the creation of Bill of Materials (BOMs)
  • Experience with electronic scheduling systems (such as Smartsheets, Planet Together, Orchestrate, RTMS)
  • Experience with PowerBI or Tableau
  • Supply Chain certifications or project management certification (ASCM, PMP)
What we offer:
  • 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
  • health benefits to include medical, prescription drug, dental and vision coverage
  • bonus target of 10.0% of the base salary
  • relocation assistance may be available

Additional Information:

Job Posted:
February 20, 2026

Expiration:
February 25, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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