Business Transformation Analyst

🔥 12 minutes ago

🐎 Kentucky – Remote

🐎 Kentucky – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧐 Analyst

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• 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

• 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

• 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