Senior Project Manager – CQV / Process Engineering

OverviewWe are seeking a Senior Project Manager with a strong background in Process Engineering and CQV to support capital and operational projects at a leading biopharmaceutical facility in Bend, Oregon. This individual will drive projects involving process systems, equipment, and facility improvements within a GMP environment.Key ResponsibilitiesLead project execution for process engineering, equipment, and facility-related initiativesManage timelines, budgets, risks, and deliverables across multiple workstreamsCollaborate with process engineers, validation teams, quality, and manufacturingOversee commissioning, qualification, and validation (CQV) activitiesEnsure compliance with GMP, FDA, and regulatory standardsSupport process improvements, tech transfer, and scale-up activitiesInterface with vendors, contractors, and internal stakeholdersProvide consistent project updates and reporting to leadershipRequired Qualifications10+ years of project management experience in life sciencesStrong background in process engineering, CQV, or bothExperience managing projects in biotech, pharmaceutical, or biologics environmentsSolid understanding of equipment, utilities, and manufacturing processesDemonstrated experience in GMP-regulated environmentsStrong organizational and leadership skills with technical depthPreferred QualificationsPMP certification preferredHands-on experience with CQV (IQ/OQ/PQ) execution and oversightExperience with process validation, tech transfer, or PPQFamiliarity with biologics manufacturing processes (upstream/downstream)