Validation Engineer

ResponsibilitiesDraft and implement Quality System documentation designed to establish good validation practices within the organization.Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards.Support all stages of qualification of Analytical Instrument and Manufacturing equipment.Support all stages of qualification of automated manufacturing equipmentConduct Analytical Instrumentation Qualifications in accordance with USP and Vertex SOPs.Conduct Automation Assessments to ensure compliance with 21 CFR Part 11.Coordinate with vendor personnel to schedule and execute of test plans, if required.Coordinates with the internal stakeholders to safely and effectively schedule CQV activities, whenever required.Effectively works with cross departmental stakeholders, including but not limited to information services, EH&S, Global Security, design teams, and quality.Author documents related to or support process validation related activities that include but not limited to aseptic process simulations (APS), process performance qualification, material qualifications, etc.Develop cycles for sterilization processes and validate them, if pletes assigned training and ensures that they are 100% compliant 100% of the time.Ensure that all Validation activities align with the current SOPs, global standards and cGMP guidelines.Supports right-the-first time culture for all documents distributed across the organization. Ensure the Validation team reputation and partnership is flourished with the cross-functional teams.Ideal candidatesDemonstrated ability to safely execute Validation activities in a dynamic fast paced environment.Experience developing and executing Validation protocols in a GMP Manufacturing and Analytical Laboratory areas.Receptive to change – Adapts (quickly) to changing circumstances.Flexibility for off-shift hours, including weekend and night shift work.B.A, B.S. in Engineering or related discipline with 5-8 years of Validation experience or equivalent professional experience.Understanding and application of technical principles, theories, and concepts in the field, GMP, ISO, GAMP, ANSI.Seniority levelAssociateEmployment typeContractJob functionInformation TechnologyIndustriesPharmaceutical Manufacturing and Biotechnology ResearchBoston, MA$42,000.00-$50,000.00 #J-18808-Ljbffr

Created: 2025-09-17