Quality Data Services Specialist – Pharma QC & Data

MSD UK; Wilson (NC); On-site; USD 87,000 - 137,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) retirement plan

Paid holidays & vacation

Job summary

Merck is seeking a Growth and Improvement-minded Data Services Specialist in Quality Control to support stability data review, plant site release, and site APR reviews. The role demonstrates mastery of data management systems such as GLIMS, MEDS, IPI, and SAP, and ensures GMP compliance while collaborating across NASU teams and external partners.

The position emphasizes problem solving, process improvement, and adherence to FDA regulations, with opportunities to influence a cross-functional team

Qualifications

• Bachelor of Science degree, preferably in Chemistry, Biology, or Engineering with ≥ 2 years in a pharmaceutical laboratory setting
• Knowledge and experience with data management and documentation programs (GLIMS, MEDS, IPI, SAP, etc.)
• Prior experience in a pharmaceutical laboratory setting
• Adaptability, Analytical Instrumentation, Analytical Method Development, Dissolution Testing, Driving Continuous Improvement, GMP Compliance, Karl Fischer Titrations, Laboratory Documentation, Laboratory Safety, Microbiological Analysis, Microbiological Test, Teamwork, Technical Writing, Troubleshooting, Use of Laboratory Equipment

Responsibilities

• Stability lab data review, plant site release, and review of site APR
• Data trending and support of Quality Notifications and CAPAs
• Support GLIMS updates; review builds and IPI specification verification
• Review of technical memos and testing protocols
• Attend departmental meetings and serve as liaison between NASU teams and external entities

Job description

Merck is seeking a Growth and Improvement-minded Data Services Specialist in Quality Control to support stability data review, plant site release, and site APR reviews. The role demonstrates mastery of data management systems such as GLIMS, MEDS, IPI, and SAP, and ensures GMP compliance while collaborating across NASU teams and external partners.

The position emphasizes problem solving, process improvement, and adherence to FDA regulations, with opportunities to influence a cross-functional team