Sr. Recipe Author

What You Will Achieve

The recipe author will become proficient with the standard functionality of MES (Manufacturing Execution System) PharmaSuite and work with production units to convert paper records to EBR (Electronic Batch Record). They will focus on directly authoring and configuring master batch record and templates revisions validation and change controls of EBR Recipes at the Kalamazoo Manufacturing Site. The recipe author will have knowledge of SAP Functions including BOM PV and IDOC management to assist in troubleshooting issues. The recipe author will define and analyze business requirements through meeting with production units and develop detailed designs to meet those requirements. They will direct the coordination of standard work practices assuring alignment of supporting systems and reports. They will provide training to production units troubleshooting as well as ongoing data management for production this role it is critical to be on-site engaging with operations on a regular basis to ensure understanding of processes and gathering critical parameters as well as supporting hypercare for go-live activities. The recipe author will need to have a proactive approach in managing their time and engaging the production units.

How You Will Achieve It

• Responsibilities can include but not limited to:
  Manage Electronic Batch Record (EBR) design and configuration changes change control updates process reviews and alignment with associated documentation used to the lifecycle procedure.
• Facilitate lead and participate in process mapping of business processes.
• Engagement of SMEs Leads and Operators to ensure critical parameters are being captured.
• Support end users on EBR execution and usage through training super users (as applicable).
  Be the first point of contact for electronic batch record manufacturing issues as part of sustainment team and escalate to leadership as needed.
• Background in automation integration requirements and systems to be able to support Edge Gateway OPC Tunnelor and other automation capabilities integrated with MES.
• Having thorough knowledge of MES recipe design baseline configuration writing and executing functional verification reports.
  Handling of Shop floor troubleshooting in SAP - AMPS interface for Electronic Batch Records.
• Management of IDOCs
• BT ticket follow ups and ensuring its resolution with EBR Issues.
• Ensure all the performed activities comply with respective area procedures.
• Identify deviations/exceptions and escalate to leadership by appropriate procedures.
• Adherence to safety procedure GMP and GDP practices.
• Reassess and participate in an agile change environment to enhance the process at intervals to eliminate non-value-added activities and drive continuous improvement including supporting projects and deployments.

• Participate in cross functional teams to support enhance and upgrade AMPS.
• Technical document writing for procedures jobaids and functional verification protocols creation and execution.
• Assist in the work required to train execute track and reporting duties for other colleagues of the EBR team.

Quality Management and Compliance:

• Ensure compliance of operations to cGMP safety and Pfizer integrity principles at all stages of activity
• To participate in internal & external (regulatory & non-Regulatory) audits.
• Assist Manager in tracking EBR procedure updates periodic review of EBR procedures and emergency changes as required.

Training:

• To attend the training of all applicable procedures as per schedule.
• Colleague will be responsible for cross training to be able to support all AMPS areas being deployed or sustained.
• To develop and update content for AMPS EBR training for new hires to the EBR recipe authoring team.

Here Is What You Need (Basic Requirements)

• Applicant must have a bachelors degree with at least 2 years of experience; OR a masters degree with 0 years of experience;
  OR an associates degree with 6 years of experience; OR a high school
  diploma (or equivalent) and 8 years of relevant experience.
• Computer Skills: SharePoint Proficiency in Microsoft office suite products (Word Excel Power point)
• Language Skills: Effective oral and written communications skills

Bonus Points If You Have (Preferred requirements)

• Pharmaceutical experience
• Certifications: M1 Yellow Belt and/or Pfizer Human Performance methodology.
• Computer Skills: EBR Recipe Design and Authoring PharmaSuite AMPS (MES) HTML Java or object oriented programming.
• Focused in Systems Analyst/Data Management.
• Experience working in Quality Tracking Systems.

PHYSICAL/MENTAL REQUIREMENTS

• Ability to perform mathematical calculations and ability to perform complex data analysis
  NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
  Occasional travel may be required (<5%)
• In this role it is required to be onsite 5 days a week

Work Location Assignment:On Premise

Last Date To Apply: May 4 2026

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.