Senior Validation Project Lead/Manager

Job : Senior Validation Project Lead/Manager Location : Virginia or Maryland or North Carolina What You’ll Do Support Client commissioning / validation for facility, utility, equipment, cleaning and process validation projects Prepare and execute commissioning / validation lifecycle documents Participate in any stage of clinical or commercial production including green field construction, facility renovation, new product development, product launch, or product/process upgrade Write summary reports for validation and qualification protocols Support project milestones, priorities and deadlines Write operating procedures for technical equipment and practices and procedures Perform system and process risk assessments and analyses Schedule and coordinate protocol execution with other departments including manufacturing, facilities and project management Develop project specific validation plans and strategy Able to manage and execute multiple projects to meet client’s priorities Provide a practical approach to problem solving Individuals must represent Compli at client sites and interact confidently with clients, contractors, management and peers Other duties as assigned What You’ll Bring Must have minimum 7 years CQV experience with aseptic liquid fill facilities, utilities, equipment and systems. Bachelor’s degree in a related life sciences or requisite industry training and experience Ability to converse about scientific matters Ability to work independently or in collaboration with others In depth understanding and application of validation principles, concepts, practices and standards Considered a Subject Matter Expert (SME) in one area of validation Proficient in current Good Manufacturing Practices and other applicable regulations Experienced with all pertinent industry best practices (e.g., ISPE) including development and execution of all applicable system life cycle deliverables (e.g., URS, SRS, FRS, DDS, RTM, Unit, Integration, User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report Demonstrated expertise in at least one aspect of system qualification and regulatory compliance (e.g., EMEA, GCP, GLP, GMP, QSR) and internal requirements employing regulatory guidance and industry standards Excellent written communication skills with emphasis in technical writing Proficient in Microsoft Word, Excel, Power Point and Project Travel Local to Virginia or Maryland or North Carolina areas. Travel to the East Coast or Midwest for extended on-site services. This role is not open to C2C staffing. At Compli, we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender identity, gender expression, disability, veteran status, pregnancy status, or any other status protected by law. #J-18808-Ljbffr GBA