Pharmaceutical Master Data SpecialistWest Lothian, Scotland
Do you currently work in a pharmaceutical or a related industry as a Master Data Specialist? Have you used JD Edwards orTrackWise? 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 Specialiston 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 Specialistrole 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.
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Pharmaceutical Master Data Specialist employer: Medical Update Online
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