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QA Validation Specialist – Lab 6 mth contract

icon building Company : Test Triangle
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Job Description - QA Validation Specialist – Lab 6 mth contract


QA Validation Specialist – Lab 6 mth contract

Summary: QA Validation role to ensure Qualification of LIMS and Laboratory instruments is performed in compliance with regulatory requirements, company policy and procedures. 

 

Key Responsibilities:



  • Support the introduction, implementation, and lifecycle management of LIMS, Empower and other Lab software within QC and analytical laboratories.

  • Serve as QA Validation SME, overseeing Computer System Validation (CSV) activities, including URS, FS, RA, IQ, OQ, PQ, and validation reports.

  • Ensure compliance with EU GMP, FDA, EMA, and Annex 11 standards for electronic systems.

  • Collaborate with Quality, QC, Manufacturing, IT, and Regulatory teams to optimize lab workflows supporting product testing.

  • Support integration of analytical instruments and other quality systems with LIMS.

  • Provide user training, troubleshooting, and continuous improvement support for lab personnel.

  • Drive change control, deviation management, and periodic review processes related to LIMS and associated systems.

  • Maintain audit readiness, ensuring documentation and processes align with corporate and regulatory requirements.

 

Qualifications & Experience:



  • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, Biotechnology, Life Sciences, or IT/Computer Science.

  • 5+ years’ experience in the pharmaceutical/medical device industry with a focus on QC laboratory software, LIMS implementation, and validation or Empower upgrades.

  • Strong expertise in CSV methodology, validation protocols, and regulatory frameworks.

  • Comprehensive knowledge of cGMP, pharmacopeial standards (USP, EP, JP), and global regulatory guidelines (FDA, EMA).

  • Skilled in equipment and analytical instrument qualification, calibration, and validation maintenance.

  • Excellent documentation skills, including accurate preparation and maintenance of SOPs, validation protocols, and technical reports.

  • Proven project management abilities, ensuring adherence to timelines, budgets, and quality standards.

  • Deep understanding of data integrity principles, validation documentation, and regulatory compliance.

  • Effective problem-solver in validation challenges, providing practical and risk-based solutions.







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