Business Transformation Analyst

Thermo Fisher Scientific

. Perform complex reviews of laboratory database content for compliance with validation documentation, SOPs, business requirements, and source documentation .

Posted 10/14/2026full-timeRemote • Kentucky • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in database management, quality control, and compliance within laboratory environments, with a strong focus on data accuracy, documentation, and process improvement. Proficient in utilizing analytical skills to resolve discrepancies and enhance database services while effectively communicating technical information to diverse stakeholders.

Highest-signal resume keywords

Database ManagementQuality ControlData AnalysisRegulatory ComplianceChange Control

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Data ManagementDatabase OperationsQuality AssuranceData Quality PrinciplesSQLReporting ToolsToxicity GradingValidation DocumentationChange Control ProceduresData Integrity

Soft Skills

Attention to DetailAnalytical SkillsProblem-SolvingOrganizational SkillsCommunication Skills

Tools & Technologies

Microsoft ExcelPower BITableauLaboratory Information SystemsData Governance

Industry Keywords

Laboratory OperationsPharmaceuticalBiotechnologyClinical ResearchHealthcare

Tech Stack

Tools & technologies

SQLTableau

About the role

Key responsibilities & impact

Perform complex reviews of laboratory database content for compliance with validation documentation, SOPs, business requirements, and source documentation
Conduct technical and quality-control reviews of database modification and addition requests
Identify discrepancies, incomplete information, or requestor errors and coordinate resolution
Implement approved database updates according to change-control and database procedures
Maintain documentation of database changes for traceability, compliance, and audit readiness
Review custom reports and database outputs for completeness and accuracy
Research and respond to questions regarding laboratory database content using approved references, clinical standards, peer-reviewed literature, and other documentation
Investigate, document, and resolve database-related quality events and discrepancies
Draft communications concerning database changes, reference ranges, custom alerts, quality issues, and business requirements
Enter, maintain, and verify data in laboratory databases, applications, trackers, and metrics repositories
Maintain and revise toxicity grading content, including master toxicity tables and coding quality-control reviews
Coordinate with departments and stakeholders during database updates and implementation activities
Recommend enhancements to database services, procedures, processes, controls, and tools
Participate in process-improvement initiatives
Monitor operational activities and maintain performance metrics
Serve as a subject-matter resource for database processes and content
Train new team members and global staff on laboratory database processes, procedures, and tools
Perform other duties as assigned

Requirements

What you’ll need

Advanced degree in a relevant field with no prior professional experience required, or bachelor’s degree with at least 2 years of relevant experience
Relevant experience may include data management, database operations, laboratory operations, quality, analytics, clinical data, or related fields
Experience in a regulated, laboratory, pharmaceutical, biotechnology, clinical research, healthcare, or other quality-controlled environment preferred
Equivalency through a combination of appropriate education, training, and/or directly related experience may be considered
Strong attention to detail and ability to review complex data for accuracy, completeness, and consistency
Experience with structured databases, data-management systems, or enterprise applications
Ability to identify discrepancies, investigate root causes, and coordinate resolution of data-quality issues
Understanding of data quality, documentation, and change-control principles
Ability to interpret and follow SOPs, validation documents, technical requirements, and controlled procedures
Strong analytical and problem-solving skills
Ability to evaluate technical information and make evidence-based recommendations
Organizational and time-management skills with ability to manage multiple priorities and implementation timelines
Excellent written and verbal communication skills
Ability to communicate technical or scientific information clearly to technical and non-technical stakeholders
Ability to work independently while collaborating across functions and global teams
Ability to maintain accurate records and documentation in a quality-controlled environment
Proficiency with Microsoft Excel and other Microsoft Office applications
Preferred: laboratory information systems, clinical databases, reference-range management, quality-control review, validation, change control, deviation management, quality-event investigations, clinical laboratory reference ranges, pediatric reference ranges, toxicity grading, scientific or medical reference materials, SQL, reporting tools, database querying, data-analysis applications, Power BI, Tableau, process improvement, workflow optimization, operational metrics, SAP, Salesforce, data governance, data integrity, and technical-system training

Benefits

Comp & perks

Global organization with opportunities to collaborate with industry-leading experts
Career growth and continuous development environment
Accessibility services and accommodations for job seekers with disabilities during the application process