Technical Project Manager

Technical Project Manager – Controls & Data SystemsLocation: Northridge, CA (100% on-site) Reports To: Senior Manufacturing Operations Manager – MSAT Duration: 6-Month W2 Assignment (Potential to Extend or Convert) Pay Rate: $78/hourA global organization specializing in advanced drug delivery systems partners with leading pharmaceutical companies to develop and manufacture complex combination products, including transdermal patches and inhalation therapies.Role OverviewWe are seeking a Technical Project Manager with a strong engineering background and proven project management experience to lead initiatives involving control systems, data acquisition, and pharmaceutical manufacturing processes. This role supports late-stage development, technical transfer, and commercialization, with a focus on execution, compliance, and client engagement.Key ResponsibilitiesProject Management & LeadershipLead technical projects from initiation through completion, ensuring alignment with scope, schedule, and budgetDevelop and maintain project plans, risk assessments, and resource strategiesCoordinate cross-functional teams across R&D, Quality, Regulatory, and OperationsEnsure compliance with GMP, FDA, and regulatory requirementsTechnical ExecutionOversee design, implementation, and optimization of control systems and data acquisition platformsSupport technical transfer activities for pharmaceutical manufacturing programsGuide system integration, testing, and validation effortsApply Quality by Design (QbD) principles and statistical tools (DoE, FMEA, Gage R&R)Client & Stakeholder EngagementServe as the primary point of contact for clients throughout the project lifecycleLead project kick-offs, technical reviews, and issue resolutionClearly communicate technical concepts to internal and external stakeholdersSupport client audits and regulatory inspectionsContinuous ImprovementIdentify opportunities to improve process robustness, product quality, and efficiencyContribute to Lean initiatives and best practice implementationQualificationsBachelor's or Master's degree in Engineering (Chemical, Mechanical, Electrical, Biomedical, or related)PMP certification (or equivalent) required7+ years of experience in pharmaceutical manufacturingExperience managing technical projects in regulated or CDMO environmentsStrong background in control systems, automation, and data acquisitionKnowledge of cGMP and regulatory requirementsExcellent communication, leadership, and stakeholder management skillsPreferred SkillsExperience with transdermal patch or inhalation (MDI) manufacturing processesFamiliarity with coating, laminating, die-cutting, or filling/crimping operationsExperience supporting CMC documentation for regulatory submissions (NDA/ANDA)Lean Six Sigma or continuous improvement certificationPlease submit your resume in Word or PDF format to be considered.