Sr. Recipe Author

Scorpion Therapeutics; Michigan; On-site; USD 90,000 - 110,000; Full time

Benefits offered by this job

401(k) with matching and retirement

Paid vacation/holidays/personal days

Paid caregiver/parental and medical

Job summary

Scorpion Therapeutics is hiring for a role focused on electronic batch record (EBR) design and support within our manufacturing support team. You will author EBR recipes, convert paper records to digital formats, and help ensure alignment with lifecycle documentation.

The position emphasizes collaboration with SMEs, operators, and support teams to optimize EBR configuration, troubleshooting, and compliance with cGMP and safety standards.

Qualifications

• Bachelor's degree or higher in a relevant field.
• Experience with EBR design/authoring and MES systems is preferred.
• Strong communication skills and ability to collaborate with SMEs/leads/operators.

Responsibilities

• Author and configure 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 and lifecycle documentation alignment.
• Lead process mapping with SMEs/leads/operators to capture critical parameters.
• Support end users with EBR execution and usage; act as first point of contact for manufacturing issues.

Skills

Communication

Oral and written communication

Education

Bachelor's degree

Master's degree

Associate's degree

High school diploma

Tools

SharePoint

Microsoft Office

PharmaSuite

AMPS (MES)

HTML

Java

Object-oriented programming

Data management

Job description

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 escalated 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 escalated.

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.