Computer Systems Validation Specialist III

Computer Systems Validation Specialist III Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. They conduct risk assessments, review change requests and test scripts, draft protocols, and oversee GMP documentation revisions. This role acts as the QA CSV representative for small and large-scale projects while providing technical guidance and mentorship to junior team members. What you will get A collaborative and inclusive work environment. Opportunities for career growth and development. Access to cutting-edge technologies and tools. Competitive compensation and benefits package. 401(k) matching plan. Supportive leadership and mentoring. Commitment to ethical and sustainable practices. Our full list of global benefits can be found here: What you will do Perform all aspects of QMS process – Change Control, Deviations, CAPAs. Perform Gap assessments to identify gaps in processes and suggest remediation plans. Initiate the right quality records (Deviations and CAPAs) to drive remediation, as needed, and execute all responsibilities as CSV project lead for projects. Author/Review/Approve all end-to-end computer system validation lifecycle deliverables and activities. Schedule qualification activities and personnel to meet business, manufacturing, engineering and quality objectives. Revise and maintain SOPs to ensure continuous improvement and compliance with group/corp procedures. Perform review of engineering documents (P&IDs, SOPs, specifications, submittals, etc.). Support validation requests as a CSV SME during customer audits and inspections. What we are looking for Bachelor’s degree in computer science, engineering, or related field. At least 3+ years of experience in computer systems validation. 3+ years of experience working in a cGMP facility. Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to computer systems validation (especially for analytical computerized systems). Works independently and in teams. Background in biotech, pharma, or medical device industry. Ability to work independently and on-site in Portsmouth, NH. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now. #J-18808-Ljbffr Dormont Manufacturing Company