Hiring: QA Validation Associate Company: Randstad USA Location: Thousand Oaks, CA Job Posted Time: 2026-09-10 12:19:42 Employment Type: On-site About the job Experience: •Proficiency in electronic document management systems (e.g. Veeva, Kneat, ALM) Required Skills: •Lead and oversee reviewing validation documents, against Standard Operating Procedures (SOPs) for accuracy and compliance with procedures, based on regulatory requirements and internal guidelines. •Review from a quality perspective the validation documentation required to assure the proper development of a project and support regulatory submissions. •Provide validation expertise and support for the development (or modification phases) of manufacturing facility, utilities, systems, process and information and Computerized System; address, include and implement all the applicable QA requirements. •Participate in the risk assessment related to the project. •Assure requirements traceability throughout the whole project life cycle. •Provide support in all quality-related issues, including GMP regulations •Maintain project metrics to communicate risk trends and implementation readiness to support project timelines and commercial readiness •May perform other duties as assigned. Qualifications: •Bachelor’s Degree in Biotechnology, Microbiology, Pharmacy or equivalent. •At least 5 years of experience in Pharmaceutical, Biopharmaceutical or related manufacturing environment, or an advanced degree. Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!