Project Manager - Pharmaceutical Technical Services & Manufacturing Sciences (Tech Transfer)

Job Title: Project Manager - Technical Services & Manufacturing Sciences (Tech Transfer) Location: ONSITE - Indianapolis,IN Work Arrangement: Long-Term Contract W2/1099/C2CAbout the Opportunity Join the Technical Services and Manufacturing Sciences team of a global pharmaceutical organization as it expands to support new products moving from development into clinical and commercial supply. You will bring structure and momentum to tech transfer projects, so externally manufactured APIs, intermediates, and starting materials arrive safely, on time, and to a consistent quality standard.What You'll DoBuild and run integrated project plans, schedules, and milestones for tech transferManage scope and formal change controlCoordinate tech transfer, PPQ, batch release, scheduling, supply chain, and shipmentsSupport facility design, construction, and commissioning and qualification (C&Q)Keep internal teams and contract manufacturers aligned and accountableMaintain risk registers, dashboards, scorecards, decision logs, and action trackersGive leadership clear status reports and recommendationsKeep collaboration platforms (e.g., Teams, SharePoint) currentContribute to continuous improvement and Lean initiativesWhat You'll BringBS in Chemical Engineering, Science, Engineering, or a project management-related field3-4+ years in pharma manufacturing operations, tech transfer, or project managementAbility to independently build complex project plans in MS Project and Jira, including critical path, risk registers, and change controlExperience managing cross-functional and cross-company stakeholdersStrong problem-solving skills, including root cause analysis and corrective actionClear communication with technical and leadership audiencesAdaptability in a fast-moving, multi-priority environmentTeam-based work experienceNice to HaveMS, MBA, or Master's in Project Management; PMP or Six Sigma Green/Black BeltHands-on experience with large molecule, peptide, or small molecule manufacturingCapital project or commercialization project experienceExposure to validation, tech transfer, CMC, GMP, Quality, or HSETrack record of influencing across business functions Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions. If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.