Pharma Master Data Specialist (JD Edwards) - 12m Contract

Quality Start; Dunfermline; On-site; GBP 19,000 - 21,000; Full time

Job summary

Quality Start is seeking a Pharmaceutical Master Data Specialist to join a global pharmaceutical manufacturing team in West Lothian, Scotland on a 12-month contract. You will independently execute Master Data Management processes in a GMP environment, focusing on data accuracy and adherence to SOPs across supported systems.

Key duties include creating and approving Item and Location Masters in JD Edwards, handling Client/Study Codes in Prisym, and processing data revisions via TrackWise.

Qualifications

• Bachelor's degree or equivalent required in a relevant field.
• 0-3 years of relevant clinical supply, master data, project support, pharmaceutical, biotech, or equivalent business experience preferred.
• Detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance.
• Computer literate, with experience using spreadsheets, word processing programs, and business system tools.
• Willingness to travel preferred.

Responsibilities

• Generate and approve standard Item Masters, Item Branches, and Item Revisions within JD Edwards under established procedures.
• Generate and approve Location Masters and Location Master Revisions within JD Edwards under established procedures.
• Generate and approve Client Codes and Study Codes within Prisym under established procedures.
• Generate and approve Customer and Equipment Setup.
• Raise required Change Controls in Global TrackWise to support approved data revisions under established procedures.
• Perform assigned master data activities with accuracy and timely turnaround.

Skills

Master Data Management

JD Edwards

TrackWise

Data integrity

GMP

Attention to detail

Education

BSc in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent

Tools

JD Edwards

Prisym

Global TrackWise

Job description

Quality Start is seeking a Pharmaceutical Master Data Specialist to join a global pharmaceutical manufacturing team in West Lothian, Scotland on a 12-month contract. You will independently execute Master Data Management processes in a GMP environment, focusing on data accuracy and adherence to SOPs across supported systems.

Key duties include creating and approving Item and Location Masters in JD Edwards, handling Client/Study Codes in Prisym, and processing data revisions via TrackWise.