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Job Description

Job Description

A QMS Validation Specialist in the Life Sciences industry is responsible for ensuring that Quality Management System (QMS) software operates accurately, securely, and in compliance with strict regulatory standards . They bridge the gap between IT solutions and Quality Assurance (QA).

Responsibilities

Core Responsibilities

  • Validation Documentation: Create, review, and execute validation lifecycle documents, including Validation Plans (VP), User Requirement Specifications (URS), Functional Requirements Specifications, Traceability Matrices (RTM), and Test cases for IQ/OQ/PQ.
  • Regulatory Compliance: Ensure QMS systems align with global life science regulations like FDA 21 CFR Part 11 (electronic records and signatures), EU Annex 11, and GAMP 5 guidelines for software validation.
  • Risk Management: Conduct risk assessments (e.g., FMEA) to identify and mitigate compliance or data integrity gaps.
  • Change Control & CAPA: Manage software changes, deviations, and Corrective and Preventive Actions (CAPA).
  • Training & SOPs: Develop training materials and Standard Operating Procedures (SOPs) to ensure end-users utilize the QMS software securely and compliantly.
  • Audit Support: Act as the Subject Matter Expert (SME) during internal audits and external regulatory inspections regarding the QMS implementation.

Qualifications

Key Technical Qualifications

  • Education: Bachelor's degree in Life Sciences, Biotechnology, Computer Science, or Engineering.
  • Software Platforms: Familiarity with modern enterprise QMS platforms like TrackWise Digital, Veeva Vault Quality, MasterControl or ValGenesis.
  • Validation Frameworks: Deep practical knowledge of GAMP 5, data integrity principles, and electronic signatures regulations.

Soft Skills

  • Strong analytical and technical writing capabilities.
  • The ability to translate complex IT and quality concepts into understandable terms for cross-functional stakeholders.
  • High attention to detail with an ability to manage multiple validation projects simultaneously.

About Us

Honeywell Technologies is a global, pure-play automation company with a legacy of innovating to help solve the world's most mission-critical challenges, enhancing the quality of life for people and communities around the world. We serve the building, industrial and process sectors with a broad portfolio of services, solutions and products, underpinned by our Honeywell Technologies Accelerator operating system and Honeywell Technologies Forge intelligence layer. By combining the deep domain expertise of our more than 50,000 employees with decades of data from our global installed base, we are uniquely positioned to lead the industrial sector's transition from automation to autonomy.

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Key Skills

Deep practical knowledge of GAMP 5 data integrity principles

Familiarity with modern enterprise QMS platforms

Validation Documentation

Training SOPs

Change Control CAPA