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17 hours ago
Job Title: System Validation and Testing Specialist
We are seeking a seasoned professional with hands-on experience in pharmaceutical quality systems, including Trackwise, Labware LIMS, and Documentum D2.
Key Responsibilities:- Lead validation efforts for the platforms to ensure regulatory compliance and GxP requirements.
- Develop and execute test strategies, protocols, and scripts to validate system functionality.
- Conduct impact assessments and lead UAT support and defect triage.
- 5+ years of experience in QA/QC systems in the life sciences/pharmaceutical domain.
- Proficiency in Trackwise, Labware LIMS, and Documentum D2 platforms.
- Solid understanding of GAMP 5, FDA 21 CFR Part 11, and CSV best practices.
We offer a dynamic work environment where you can utilize your expertise to drive business growth and excellence. This is an exciting opportunity for a motivated professional to take on new challenges and contribute to the company's success.
To be considered for this role, please submit your resume and cover letter outlining your relevant experience and qualifications. We look forward to hearing from you
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