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Thermo Fisher Scientific

Data Reviewer – Cell Lab

Thermo Fisher Scientific

. Support Cell Laboratory teams in ensuring the integrity and quality of laboratory and chromatographic data and reports .

Posted 10/15/2026full-timeRemote • IrelandJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in QA/QC analytical processes, ensuring compliance with GLP and GMP standards while effectively communicating findings and advocating for quality improvements. Proficient in reviewing laboratory data and reports, with a strong attention to detail and ability to provide clear feedback.

Highest-signal resume keywords
QA/QC Analytical ExperienceKnowledge of GLP and GMPCell-Based AssaysLaboratory Procedures and MethodologyStrong Verbal and Written Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Analytical Data ReviewChromatographic Data AnalysisSOP KnowledgeData Quality MonitoringProcess Improvement Initiatives
Soft Skills
Attention to DetailClear Feedback CommunicationCollaboration with Laboratory StaffAbility to Work Under Pressure
Tools & Technologies
Laboratory NotebooksStandard Office EquipmentData Entry Databases
Industry Keywords
Quality ControlGood Laboratory PracticeGood Manufacturing PracticeFederal RegulationsAnalytical Methods Compliance

About the role

Key responsibilities & impact
  • Support Cell Laboratory teams in ensuring the integrity and quality of laboratory and chromatographic data and reports
  • Ensure analyses follow validated or experimental analytical procedures and compare results against methodology, protocol and product specifications, SOP acceptance criteria, and GMP
  • Review data entered into databases and reports and monitor laboratory data quality
  • Ensure the quality of laboratory data and reports
  • Review chromatographic data, related notebooks, and sample results for scientific soundness, completeness, accurate data representation, and final reported results
  • Evaluate data for compliance with analytical methods, client criteria, GLP, and GMP
  • Deliver clear and concise review findings, noting deficiencies in analytical data or reports
  • Communicate with laboratory staff to proactively address laboratory documentation quality
  • Prepare QC statements noting deficiencies in analytical data sets or notebooks
  • Report deficiencies to the project leader for correction
  • Facilitate conversations with laboratory staff about best documentation practices and quality findings
  • Advocate for quality and review process changes
  • Identify and support process improvement initiatives

Requirements

What you’ll need
  • BSc in Science or related field required
  • 2+ years of QA/QC analytical experience, including thorough knowledge of cell-based assays and experience reviewing analytical data/results
  • Thorough knowledge of SOPs and Federal Regulations, including GLP and GMP
  • Strong verbal and written communication skills
  • Strong technical knowledge of laboratory procedures, methodology, and standards
  • Ability to independently review laboratory reports and analytical methods
  • Strong attention to detail
  • Ability to provide clear and concise feedback and/or documentation of results
  • Ability to communicate, receive, and understand information and ideas with diverse groups of people
  • Ability to work upright and stationary and/or standing for typical working hours
  • Ability to lift and move objects up to 25 pounds
  • Ability to work in non-traditional work environments
  • Ability to use and learn standard office equipment and technology proficiently
  • May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments
  • Ability to perform successfully under pressure while prioritizing and handling multiple projects or activities

Benefits

Comp & perks
  • Fully remote work arrangement
  • Standard Monday–Friday work schedule