Veeraj Pardeshi
Sr Qa Analyst @FUJIFILM Biotechnologies
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WORK HISTORY
Sr Qa Analyst @FUJIFILM Biotechnologies
College Station, TX, US
Approving and finalizing Standard Operating Procedures, Batch Production Records, and validation protocols and reports. Reviewing Deviation Reports, Corrective Action/Preventive Action Plans, and technical data, ensuring adherence to industry and company standards. Drafting and refining internal quality policies, procedures, and reports to enhance operational efficacy. Conducting meticulous inspections of final product containers and providing thorough approval of executed process records and data. Leading Quality audit functions such as audits of lab notebooks, equipment logbooks, and vendor, supplier, and client audit questionnaires. Identifying process improvements and opportunities for enhancing Quality Systems. Providing daily guidance to ensure compliance with national and international standards and regulations. Supporting regulatory, client, and internal audits as a knowledgeable resource. Acting as a QA liaison to internal departments and external client quality groups, ensuring seamless communication and collaboration. Quickly notifying senior management of potential quality or regulatory issues impacting product quality and compliance. Offering technical oversight and training for the QA team to cultivate a robust quality culture. Assisting in compliance functions, ensuring priority tasks are addressed effectively. Escalating any quality-related issues to Quality Management and/or departmental management as required.
EDUCATION
University of Mumbai
Bachelor's degree, Mechanical Engineering
Worcester Polytechnic Institute
Masters of Science (M.S), Mechanical Engineering
ABOUT VEERAJ PARDESHI
As a Quality Assurance professional with over 7 years of hands-on experience in top-tier pharmaceutical and biotech companies like FUJIFILM Biotechnologies, Moderna, and Boston Scientific, I specialize in ensuring compliance with GMP, supporting inspection readiness, and driving continuous improvement across QA systems.My core strengths include:• Batch Record Review & Disposition• Deviations, CAPA, and Change Control• SOP Approval, GMP Documentation• Quality Floor Support & Internal Audits• Risk Management & Regulatory ComplianceI’ve contributed to end-to-end quality processes across multiple phases of production, from line clearance to documentation to audit prep. With a strong background in systems like TrackWise, Veeva, and LMS, I bring both operational insight and regulatory focus.I’m passionate about building strong quality cultures, streamlining QA workflows, and mentoring cross-functional teams toward a shared vision of operational excellence. Let’s connect!
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