Validation Engineer

Title: Validation Engineer SeniorLocation: Thousand Oaks CA Duration:12+ MonthsDescription:Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating/reviewing/executing C&Q protocols, plans, and summary reports. Works with project teams and SMEs to develop testing strategies. Participates in project meetings to inform stakeholders on progress of C&Q activities.Key Skills and Requirements:• Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV role.• Knowledge of cGMP commissioning/qualification/validation practices.• Familiarity with Kneat Gx Platform or other digital C&Q systems.• Experience working with cross-functional stakeholders.• Knowledge of quality assurance principles.• Experience working within project teams and multiple projects in parallel.• Effective communication skills, both verbal and written.• Able to think analytically with the ability to resolve issues.• Able to manage own time efficiently.Top 3 Must Have Skill Sets:Experience in commissioning/qualification/validation, experience in a GMP environment, experience with analytical instruments (Benchtop laboratory equipment)