Project Management Senior Associate

Location: Remote - Thousand Oaks, CA (EST or PST preferred)Employment Type: Contingent Worker (Contract, W2)Contract Length: 12 months (possible extension)Compensation: $52/$58 per hour (based on experience)Summary of the RoleJoin a big biopharma leader as a Supply Chain Project Manager, responsible for executing product lifecycle management activities across manufacturing, regulatory, and supply chain functions. You will translate product launch and variation strategies into actionable implementation plans and oversee change control execution for compliance. This fully remote role requires 3-5 years of experience managing change controls and lifecycle processes in a regulated industry.Key ResponsibilitiesManage change control timelines with input from Variation and Regional Operations LeadsMaintain compliance in Change Control Management systems for Global Distribution Change Records (GDCR) and Customer Facing SKU Change Records (CFSCR)Provide timely stakeholder updates on GDCR and CFSCR status and readiness activitiesRepresent the SCPM Hub in project planning, execution, and operational meetingsBuild and maintain effective relationships across key functional areasIdentify opportunities to streamline departmental activities and lead improvement projectsDevelop and implement new procedures and processes to optimize resultsShare and implement best practices with cross-functional stakeholdersAdapt quickly to changing priorities in a dynamic, global environmentIndependently execute projects and business cases as assignedRequired Experience & Skills3-5 years' experience with lifecycle management across full product manufacturing stagesExperience with change control in regulated (biotech/pharmaceutical) environmentsKnowledge of GMPs and supply chain or quality processesTrackwise or similar Quality System experienceStrong stakeholder management and cross-functional collaboration skillsExcellent communication and analytical abilitiesSelf-starter who thrives in dynamic, fast-paced settingsPreferred QualificationsASCM/APICS and/or PMP certificationTop 3 Must Have Skills1. Change Control experience in Lifecycle Management, with Trackwise or other Quality System background2. Knowledge of GMPs and biotech/pharmaceutical industry practices3. Supply Chain and/or Quality background, especially in lifecycle managementDay-to-Day ResponsibilitiesQuickly train and gain system access; independently follow SOPs and participate in project forums/meetings; gather requirements and translate them into compliant Change Control records (CFSCR or GDCR); ensure all activities are completed on schedule to support product launches and variations; actively partner with assessors and task owners to drive timely completion and regulatory compliance.Basic QualificationsMaster degreeBachelor degree and 2 years of experienceAssociate degree and 6 years of experienceHigh school diploma / GED and 8 years of experienceThis posting is for Contingent Worker, not an FTE#J-18808-Ljbffr