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Master Data Specialist at

SPECTRAFORCE

Master Data Specialist at

SPECTRAFORCE

in New Castle, New Hampshire Posted in about 8 hours ago.

Type:

full-time

Position Title:

Master Data Specialist Work Location:

101 International Drive Portsmouth New Hampshire 03801

Assignment Duration:

7 months

Work Schedule:

Regular Office Hours Work Arrangement:

Onsite Position Summary:

Responsible for the preparation, cleansing, validation, loading, and ongoing support of QC master data for gLIMS implementation. Partners with QC SMEs and project teams to ensure accurate, complete, and compliant data migration, support go-live readiness, and maintain data integrity throughout the project lifecycle.

Key Responsibilities:

• Perform local master data setup and load in alignment with global guidelines and data principles.
• Build and input all initially required master data into the global LIMS system, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.
• Conduct local data cleansing to ensure data quality and accuracy.
• Develop local work instructions to detail the execution of global processes at site level.
• Proficiency in using LIMS or similar systems and familiarity with quality standards and regulatory requirements.

Qualification & Experience:

• Degree (required): Bachelor of Science in Science related discipline or relevant experience in the field.
• Language(s)

Required:

English preferred, Ability Level 2 - Business Fluent.

Work Experience Area:

QC, Enterprise systems, Validation;

Level:

Entry Level - 0-4 years.

• Experience in data management and familiarity with master data setup and loading processes.
• Strong attention to detail and analytical skills to ensure data accuracy and quality.
• Ability to develop clear and concise local work instructions.
• Knowledge of QC lab operations and related data requirements.
• Proficiency in using LIMS or similar data management system.
• Advanced technical knowledge of Quality control and manufacturing operations.
• Working knowledge and experience with Quality Systems including deviations, change controls, CAPAs, OTNs, deviations; both the system (TrackWise) and the practical applications in operations.
• Knowledgeable in process, equipment, cleaning, and computer system validations to the extent of being able to effectively review and approve protocols and reports and support implementation of new equipment.
• Demonstrated ability to manage medium to large sized projects within required timeframes.
• Demonstrate ability for effective Planning, Organizing and Controlling competency.
• Demonstrate sound decision making.
• Ability to work inter-departmentally and with customers.
• Demonstrates role model behaviors for GMP and Safety behaviors.
• Strong written and verbal communication skills.
• Ability to work in MS Project, Word, Excel, PowerPoint.

Working Conditions & Physical Demands (If Applicable):

Work Schedule:

Regular Office Hours Travel: