Jobs · Quality Assurance · North Carolina

Validation Consultant

PM Group · Zebulon, NC · 4 days ago
On-siteQuality AssuranceFull-time
Overview The Validation Consultant position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services (OTS) team near Zebulon, NC. Outsourced Technical Services (OTS) is an integral part of PM Group’s ability to support clients across the complete project life cycle. We have over 50 years’ industry experience, strong technical knowledge and integrated resources. Clients look to us to provide experienced technical professionals that complement their project teams. Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US. The Validation Consultant will support the Project Management Office (PMO) project portfolio at an aseptic manufacturing site. This is a long-term assignment anticipated to run from December 2026 through November 2028. PM Group is an employee owned, international project delivery firm with a team of 4,000+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners. Responsibilities The role is responsible for leading validation activities across facility systems, aseptic formulation and filling, device assembly, packaging, IT systems, warehouse operations, and Quality Control (QC) environments.Resources will be assigned multiple projects based on their technical expertise and will be expected to work independently with minimal oversight following onboarding and training.The successful candidate will lead commissioning, qualification, and validation efforts throughout the project lifecycle, including the development and execution of validation documentation, risk assessments, traceability matrices, IQ/OQ/PQ protocols, process validation activities, deviation investigations, change controls, and final reports.This is a highly collaborative, hands-on role requiring regular interaction with Engineering, Operations, Quality, Automation, and Project Management teams, as well as participation in project meetings and validation-focused initiatives.Candidates should be comfortable working on-site and supporting critical project activities, including occasional evening or weekend work during major project execution phases or site shutdowns. Qualifications Pharmaceutical Validation & CQV ExperienceExperience generating and executing validation documentation in a GMP pharmaceutical environment.Ability to independently lead validation activities and deliverables.Authoring & Execution of Validation DocumentationValidation Plans and ReportsRisk AssessmentsTraceability MatricesDesign Qualification/Design ReviewIQ/OQ/PQ and Process Validation Protocols & ReportsDeviation, Change Control & GMP ComplianceInvestigation and documentation of deviationsChange Control ownership and validation impact assessmentsKnowledge of GMP, FDA, EU Annex 15, and GAMP 5 requirementsManufacturing Equipment & Aseptic ProcessingManufacturing equipment upgrades and production line modificationsAseptic formulation and filling equipment, including RABS systemsDevice assembly and packaging equipment validationAutomation & Digital Manufacturing SystemsSCADA, PLC, PAS-X, LMES, and related manufacturing systemsElectronic validation systems such as HP ALM/TIMS and Veeva QualityDocs/Vault QualityFacility, Utility & Laboratory SystemsHVAC, BMS, refrigeration, and facility utilitiesLaboratory and GMP facility modificationsProcess instrumentation, monitoring, and calibration systemsProject Execution & Stakeholder ManagementAbility to manage multiple projects simultaneouslyRegular communication with project managers regarding status, risks, and escalationsParticipation in recurring project meetings and validation leadership activities All of your information is confidential according to EEO guidelines. Why PM Group? As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2026 business strategy. Click here to read more in our 2025 Environmental, Social and Governance Report. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know. RECRUITMENT AGENCIES NEED NOT APPLY

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