Senior Validation Specialist

Job Responsibilities:You will have engineering validation oversight and engineering validation signatory responsibility for approval of commissioning, qualification/validation, and final report documentsYou will be responsible for assessing, qualifying, and validating equipment, critical systems (utilities), facilities, computer systems, and cleaning, as applicable (IQ/OQ/PQ/PV)Primary tasks include the development of protocols, coordination of validation activities, qualification/validation execution, preparing final reports, and assembly of final validationWork with Document Control function to maintain adequate records such as systems and equipment drawings, specifications, protocols, schedules, validation records and reports, etc., as required to establish control of all processes, systems and equipment.Final documents are archived and may be included in or support regulatory submissions, and made available during internal and external regulatory/compliance auditsApply thoughtful understanding of GMP, relevant SOP curriculum, routine project procedures, project management, and other trainingGenerate and review Change Control documents, site validation documents, and site Standard Operating Procedures.Lead and interface with team members (Engineering, Manufacturing, Regulatory Affairs, Quality Operations, Quality Validation, Supply Chain, and other technical disciplines) representing the respective validation elementsEmphasis is on ensuring accuracy and integrity on validation documentation meets regulatory guidelines and industry standardsWrite protocols and reports, execute validation documents regarding acceptability to industry standards (GMPs, FDA Guidelines), procedures, and regulatory requirementsUtilize Quality-Engineering tools to problem solve/troubleshoot and assist in risk analysis (e.g., FMEA, traceability matrices, Design of Experiments, QbD, SPC)Use validation test equipment to support validation activities

Qualifications:Bachelor's degree or equivalent in Biomedical, Mechanical, or Manufacturing Engineering5+ years of experience of Validation activities for Pharmaceutical manufacturingWorking cross-functionally with Production, Engineering, and QC departments

📞 Contact your Recruiter:For more information about the role and to express your interest, you can reach out to our recruiter, Lauren Keltz, directly:📧 Email: LKeltz@harbasolutions.com📱 Phone: 339-800-4995💼 About Harba Solutions:Harba Solutions is a leading scientific services firm operating across a range of scientific industries including pharmaceuticals, biotechnology, medical devices, contract research organizations, and agricultural sciences. With a substantial network of qualified scientific candidates and ongoing interactions with emerging talents, we specialize in effectively placing scientific professionals in roles encompassing laboratories, chemistry, biology, and quality-focused disciplines, to name a few. Backed by strategic investors, our core values of commitment, work ethic, team and self-ownership, craft mastery, and pursuit of success shape our mission. Explore the opportunities at Harba Solutions and become part of the evolution of scientific services.