QA Documentation Specialist I — Certification & Compliance

Gaming-Lab; Bangor; On-site; GBP 28,000 - 36,000; Full time

Benefits offered by this job

25 holidays per year, plus Bank Hollid

Pension Plan

Annual Discretionary Bonus

Monthly team lunches

Diverse workplace

Free on-site parking

Job summary

Gaming Laboratories International (GLI) is seeking a Documentation Specialist for our Bangor, North Wales office. The entry-level role supports the QA team by reviewing engineering test files for regulatory compliance, compiling certification documents, proofreading, and conducting related research.

You will maintain knowledge of submission requirements for each jurisdiction, review documentation, and troubleshoot issues using manufacturer sources and past submissions.

Qualifications

• Bachelor’s degree in English, Law or a closely related discipline

Responsibilities

• Review engineering test files for regulatory compliance
• Compile certification documents
• Proofread and conduct related research
• Support QA by following certification process and jurisdiction requirements
• Review engineering documentation and verify notations
• Obtains and reviews engineering documentation via relevant systems
• Maintains knowledge of requirements for each submission and jurisdiction
• Troubleshoots issues using manufacturer documentation and past submissions
• Uses a file tracking system (Protrack) and other systems to process QA issue reports
• Generates draft certifications using report templates
• Finalizes certifications and archives reports

Skills

Communication skills

Attention to detail

English proficiency

Multitasking

Education

Bachelor’s degree in English/Law or related

Business School or Legal Assistant Certification (preferred)

Tools

Microsoft Word

Microsoft Outlook

Microsoft Excel

Protrack

Job description

Gaming Laboratories International (GLI) is seeking a Documentation Specialist for our Bangor, North Wales office. The entry-level role supports the QA team by reviewing engineering test files for regulatory compliance, compiling certification documents, proofreading, and conducting related research.

You will maintain knowledge of submission requirements for each jurisdiction, review documentation, and troubleshoot issues using manufacturer sources and past submissions.