LIMS Master Data Analyst

We are seeking a LIMS Data Analyst II / LIMS Master Data Analyst to support the preparation, cleansing, validation, loading, and ongoing management of QC master data for a global LIMS implementation. This role will work closely with QC subject matter experts and project teams to ensure accurate, complete, and compliant data migration, support go-live readiness, and maintain data integrity throughout the implementation lifecycle. The ideal candidate will have experience with LIMS or similar systems, QC laboratory operations, data management, and quality systems within a regulated environment., * Prepare, cleanse, validate, and load QC master data for LIMS implementation.

• Perform local master data setup in accordance with global guidelines and data principles.
• Build and enter master data into the global LIMS, including consumables, sampling plans, specifications, parameter lists, test methods, and LES templates.
• Conduct data cleansing activities to ensure accuracy, completeness, and consistency.
• Support data migration and LIMS go-live readiness activities.
• Develop clear and concise local work instructions for the execution of global processes at the site level.
• Collaborate with QC SMEs and cross-functional project teams throughout implementation activities.
• Maintain data integrity and support data quality throughout the project lifecycle.
• Support applicable quality-system and validation activities.
• Ensure compliance with applicable cGMP, quality, regulatory, and safety requirements.
• Manage assigned activities and deliverables within established timelines.
• Communicate effectively with cross-functional teams and internal customers.

• Bachelor’s degree in science or a related discipline, or relevant equivalent experience.
• 0-4 years of relevant experience in data management, QC, LIMS, enterprise systems, or validation.
• Experience with master data setup, data cleansing, validation, and loading.
• Proficiency with LIMS or similar laboratory/data management systems.
• Knowledge of QC laboratory operations and related data requirements.
• Familiarity with quality systems, including deviations, change controls, CAPAs, and related processes.
• Knowledge of validation principles and experience supporting process, equipment, cleaning, or computer system validation activities.
• Strong analytical skills and attention to detail.
• Strong planning, organization, prioritization, and problem-solving skills.
• Ability to manage assigned projects and deliverables within required timelines.
• Strong written and verbal communication skills.
• Ability to work effectively across departments and with cross-functional teams.
• Proficiency in Microsoft Excel, Word, PowerPoint, and MS Project.
• Working knowledge of cGMP and applicable quality and regulatory requirements.
• Strong commitment to quality, data integrity, and workplace safety.

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy., TekWissen® Group is an equal opportunity employer supporting workforce diversity.