Analytical Validation Specialist III
Planet Pharma - louisville, KY
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Job Description: The Analytical Validation Specialist III role will assist validation activities including, but not limited to, software updates, new system introduction, and decommissioning of analytical systems. The individual will work closely with Senior Analytical Validation Specialists and other functional groups to contribute to quality, and right first time performance. This role requires closer support from other Subject Matter Experts and Management.• Develop Technical Knowledge and documentation on analytical equipment.• Provide Subject Matter Expert support for troubleshooting of analytical equipment.• Assist and support the planning and execution of validation plans involving analytical equipment changes.• Perform advanced troubleshooting and advanced helpdesk tickets (template creations, focus control etc.)• Execution of Installation QualificationsOperational Qualifications and Performance Qualifications.• Own change requests and complete change request tasks to support project completion• Assist in Generating User Requirements Specification Documentation, complete Electronic RecordsElectronic Signatures, Data Integrity Risk Assessments and Audit Trail Risk Assessments.• Review analytical equipment, manuals, and help devise validation plans• Identify Quality Issues, involve stakeholders, help drive to completionresolution• Assist in completion of Correct ActionsPreventative Actions• ReviewApprove Commissioning Qualification Validation Documents• System Acceptance Ownership and Completion• Vendor escorting as needed• Demonstrates ownership and remediation of Data IntegritySkills:• Good working knowledge on Validation deliverables and Data Integrity principles.• Working knowledge and experience with Quality Systems including deviations, change controls, CAPAs, OTNs, deviations; both the system (TrackWise) and the practical applications in operations• Knowledgeable in process, equipment, cleaning, and computer system validations to the extent of being able to effectively review and approve protocols and reports and support implementation of new equipment.• Demonstrate sound decision making.• Ability to work inter-departmentally and with customers.• Demonstrates role model behaviors for GMP and Safety behaviors• Strong written and verbal communication skills• Ability to work in MS Project, Word, Excel, PowerPointEducation:High School Diploma or Equivalent; (4 year degree strongly preferred)Pay Rate: $70-80Hr *Salary will be commensurate with candidate experience
Created: 2025-02-22