Sr. Recipe Author
Pfizer
August 07, 2026
On-site
Michigan, United States
Other
Responsibilities:
- Author and configure Electronic Batch Record (EBR) recipes in PharmaSuite/MES, including master batch records/templates, revisions, validation, and change control.
- Convert paper batch records to EBR; manage EBR design/configuration changes, updates, and alignment with lifecycle documentation.
- Lead/process map business processes; engage SMEs/leads/operators to capture critical parameters.
- Support end users with EBR execution and usage; act as first point of contact for manufacturing issues (sustainment/hypercare) and escalate as needed.
- Support troubleshooting using MES knowledge and SAP (BOM, PV, IDOC management; SAP–AMPS interface); manage IDOCs; follow up on BT tickets.
- Support automation integration capabilities (e.g., Edge Gateway, OPC Tunneler) and cross-functional AMPS support/upgrades.
- Write technical documentation (procedures, job aids, functional verification protocols); assist training and tracking/reporting for EBR team.
- Ensure compliance with cGMP/safety/GDP; participate in audits; identify deviations/exceptions and escalate.
Qualifications:
- Bachelor’s (2+ years) OR Master’s (0+ years) OR Associate’s (6 years) OR High school (8 years) in relevant field.
- SharePoint; Microsoft Office (Word/Excel/PowerPoint); strong oral/written communication.
Preferred:
- Pharmaceutical experience; M1, Yellow Belt and/or Human Performance certification.
- EBR recipe design/authoring; PharmaSuite; AMPS (MES); HTML/Java/object-oriented programming; systems analyst/data management.
- Experience in Quality Tracking Systems.
Benefits (as stated):
- 401(k) with matching and retirement contribution; paid vacation/holidays/personal days; paid caregiver/parental and medical leave; medical/dental/vision.
Work schedule/location:
- On-site 5 days/week at Kalamazoo site.
- Author and configure Electronic Batch Record (EBR) recipes in PharmaSuite/MES, including master batch records/templates, revisions, validation, and change control.
- Convert paper batch records to EBR; manage EBR design/configuration changes, updates, and alignment with lifecycle documentation.
- Lead/process map business processes; engage SMEs/leads/operators to capture critical parameters.
- Support end users with EBR execution and usage; act as first point of contact for manufacturing issues (sustainment/hypercare) and escalate as needed.
- Support troubleshooting using MES knowledge and SAP (BOM, PV, IDOC management; SAP–AMPS interface); manage IDOCs; follow up on BT tickets.
- Support automation integration capabilities (e.g., Edge Gateway, OPC Tunneler) and cross-functional AMPS support/upgrades.
- Write technical documentation (procedures, job aids, functional verification protocols); assist training and tracking/reporting for EBR team.
- Ensure compliance with cGMP/safety/GDP; participate in audits; identify deviations/exceptions and escalate.
Qualifications:
- Bachelor’s (2+ years) OR Master’s (0+ years) OR Associate’s (6 years) OR High school (8 years) in relevant field.
- SharePoint; Microsoft Office (Word/Excel/PowerPoint); strong oral/written communication.
Preferred:
- Pharmaceutical experience; M1, Yellow Belt and/or Human Performance certification.
- EBR recipe design/authoring; PharmaSuite; AMPS (MES); HTML/Java/object-oriented programming; systems analyst/data management.
- Experience in Quality Tracking Systems.
Benefits (as stated):
- 401(k) with matching and retirement contribution; paid vacation/holidays/personal days; paid caregiver/parental and medical leave; medical/dental/vision.
Work schedule/location:
- On-site 5 days/week at Kalamazoo site.