Pharmaceutical Master Data Specialist - West Lothian, Scotland

Opportunity:

Do you currently work in a pharmaceutical or a related industry as a Master Data Specialist? Have you used JD Edwards or TrackWise? Are you detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance? If yes then this is the role for you.

My client a global pharmaceutical manufacturing company are looking for a Master Data Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems.

Duties and responsibilities include:

• Generating and approving standard Item Masters, Item Branches, and Item Revisions within JD Edwards under established procedures.
• Generating and approving Location Masters and Location Master Revisions within JD Edwards under established procedures.
• Generating and approving Client Codes and Study Codes within Prisym under established procedures.
• Generating and approving Customer and Equipment Setup.
• Raising required Change Controls in Global TrackWise to support approved data revisions under established procedures.
• Performing assigned master data activities with attention to accuracy, completeness, and required turnaround times.
• Analysing and interpreting company and client documentation to determine correct data setup.
• Applying established data standards, guidelines, and SOPs in a GMP setting.

This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent on the candidate and business performance. The PAYE rate is between £13.58 - £15.60 per hour.

Skills:

To apply for the Pharmaceutical Master Data Specialist role you will have the following skills:

• Bsc in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent professional experience. APICS certification preferred.
• 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.

If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

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