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TekWissen ®

LIMS Master Data Analyst

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What they do

A Data Analyst develops computer programs to analyze large customer information databases for companies and organizations. Analyzes data to identify patterns and provide information relevant to a particular business, industry or field; analysis may be used for marketing, or to detect fraud in financial transactions, or for research. Develops computer programs to protect confidential customer information.

$85,950 / year median in New Hampshire

+9% projected growth

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Job Description

LIMS Master Data Analyst at TekWissen ® LIMS Master Data Analyst at TekWissen ® in Portsmouth, New Hampshire Posted in about 8 hours ago.

Type:

full-time

Job Title:
LIMS Master Data Analyst Location:

Portsmouth, NH, 03801

Duration:

7

Months Job Type:
Temporary Assignment Work Type:
Onsite Shift:

1st

Shift Pay Rate:

$60 to $65

Overview:

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. Summary 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.

Responsibilities:

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.

Required Skills:

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® Group is an equal opportunity employer supporting workforce diversity.