Master Data Specialist, Engineering (Onsite)

Merck; Pennsylvania; On-site; USD 90,000 - 120,000; Full time

Job summary

Scorpion Therapeutics in Pennsylvania seeks a SAP Master Data Specialist to support GMP biologics manufacturing in Vaccines and Advanced Biotechnologies Process R&D, primarily managing master data for biologic clinical supplies.

Responsibilities include creating, maintaining, and reviewing master data in SAP; ensuring data quality and compliance; collaborating with Process Staff, Engineers, and Quality; and assisting with SOPs, training, and audits during the PA to NJ site transition.

Qualifications

• > BS in Engineering, Sciences, or Business with 2+ years (or MS with 1+ year) experience.
• > strong SAP master data knowledge
• > understanding of manufacturing principles
• > excellent communication and teamwork skills

Responsibilities

• Create, maintain, and review master data in SAP
• Ensure data quality, compliance with standards, and support process improvements
• Collaborate with cross-functional teams including Process Staff, Engineers, and Quality
• Assist with SOPs, training, and audits, particularly during site transitions from West Point, PA to Rahway, NJ

Skills

SAP Master Data

Data quality

Communication

Teamwork

Education

BS in Engineering/Sciences/Business

MS with 1+ year experience

Tools

Excel

Job description

Role: SAP Master Data Specialist supporting GMP biologics manufacturing in Vaccines and Advanced Biotechnologies Process R&D, primarily managing master data for biologic clinical supplies.

Responsibilities

• create, maintain, and review master data in SAP
• ensure data quality, compliance with standards, and support process improvements
• collaborate with cross-functional teams including Process Staff, Engineers, and Quality
• assist with SOPs, training, and audits, particularly during site transitions from West Point, PA to Rahway, NJ

Requirements

• BS in Engineering, Sciences, or Business with 2+ years (or MS with 1+ year) experience
• strong SAP master data knowledge
• understanding of manufacturing principles
• excellent communication and teamwork skills
• proficiency in Excel

Preferred

• pharma/sterile manufacturing experience and MES systems familiarity

High-Value

• biologics (vaccines, therapeutic proteins)
• pilot-scale GMP production
• support for regulatory compliance and process documentation
• work in dynamic environment with cross-functional stakeholders
• temporary role based in PA with planned relocation to NJ, no travel required