Master Data Specialist

Master Data Specialist – LIMS & Quality Control

Location: Portsmouth, New Hampshire, USA

Work Arrangement: On-site

Employment Type: Contract / Contingent

Compensation: Competitive hourly rate (amount not specified)

Industry: Biotechnology | Pharmaceutical Manufacturing

About the Role

An opportunity is available for an experienced Master Data Specialist to support data management and quality control systems within a regulated biopharmaceutical manufacturing environment.

The role focuses on maintaining accurate master data across LabVantage LIMS (gLIMS), Syncade (DeltaV MES), and SAP , ensuring data integrity, regulatory compliance, and successful system implementation.

Key Responsibilities

• Maintain and validate QC master data across LIMS, MES, and SAP systems.
• Perform master data setup, cleansing, migration preparation, and validation.
• Configure and maintain sampling plans, specifications, test methods, parameter lists, consumables, and LES templates.
• Ensure compliance with cGMP regulations and data integrity standards.
• Develop and maintain standard operating procedures and local work instructions.
• Collaborate with Quality Control, Manufacturing, and global project teams.
• Support LIMS implementation, system readiness, and go-live activities.
• Identify opportunities to improve data quality, system integration, and operational efficiency.
• Maintain accurate documentation throughout the project lifecycle.

Required Qualifications & Experience

• Proven experience in master data management, data cleansing, and validation within a regulated environment.
• Strong understanding of Quality Control laboratory operations and cGMP requirements .
• Knowledge of quality management processes, including CAPA, deviations, and TrackWise .
• Experience with LabVantage LIMS / gLIMS or comparable enterprise systems such as MES or SAP.
• Bachelor's degree in a science-related discipline or equivalent relevant industry experience .
• Strong analytical, organisational, and documentation skills.
• Ability to collaborate across technical and operational teams and meet project deadlines.

Additional Information

• Fully on-site position in Portsmouth, NH.
• Contract engagement through a recruitment partner.
• Competitive hourly compensation.
• Opportunity to support quality systems and data management within biopharmaceutical manufacturing.