Contract positionStart date: MayDuration: December 2025 + extensions Location: Hybrid; Willing to travel to the US and within EuropeIndustry: Life Science Join a global company in the Life Science industry seeking an experienced Quality Risk Management Lead with a deep understanding of Computer System Validation, GxP compliance, and IT Quality Operations. This role is ideal for someone with a strong foundation in IT Quality Analysis or Operations Quality. Key Responsibilities:Lead and execute Quality Risk Assessments across GxP systems and processes.Apply knowledge of TrackWise Digital, SharePoint, and other QMS tools to facilitate effective QRM practices.Develop and implement risk mitigation strategies aligned with business and regulatory expectations.Provide valuation and impact analysis of identified risks, ensuring alignment with corporate risk tolerance levels.Design and deliver training programs and workshops to educate business stakeholders on risk awareness and best practices.Requirements:Strong expertise in CSV, GMP, GxP, and IT Quality Operations.Hands-on experience with risk assessment frameworks and compliance tools (e.g., TrackWise Digital, SharePoint).Excellent understanding of regulatory requirements such as ICH Q9, FDA guidelines, and other international standards.Familiarity with QMS and LIMS platforms.Background in IT quality analysis or operations quality with progression into Audit and Compliance.Proven ability to lead workshops, train stakeholders, and drive cross-functional risk management initiatives.Strong communication, documentation, and stakeholder engagement skills.Interested in learning more? Please reach out to me via message or email me yherrera@itrustpartnering.com
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