Project manager CI Inspection

Job Title: Project manager CI InspectionLocation: Swiftwater, PAAbout The JobThe Project Manager of Continuous Improvement plays a key role in identifying, gaining consensus on, and resolving issues related to safety, compliance, and efficiency that impact the FFIP (Formulation, Filling, Inspection, and Packaging) Platform. This role contributes as a member of cross-functional teams supporting the FFIP platform and serves as a liaison between the FFIP platform and the Technical Community particularly the Portfolio Management Strategy (PMS) group, Engineering, Maintenance, and Manufacturing Science and Technology (MSAT).The ideal candidate is results-oriented, with a strong continuous improvement mindset and the ability to manage multiple projects and priorities effectively. Success in this role requires strong analytical and problem-solving capabilities, as well as a collaborative and proactive approach to project execution. These competencies are essential for driving impactful improvements across the FFIP landscape and ensuring alignment with technical and operational goals.About SanofiWe deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.Main ResponsibilitiesServes as an individual contributor and active member of cross-functional teams supportingFFIP department and Continuous Improvement projects.Leads and supports continuous improvement initiatives across the department.Provides project management support to cross-functional teams to ensure timely andActs as the department interface for resolving project-related issues and facilitatingDrives project deliverables across the FFIP (Formulation, Filling, Inspection, and Packaging)Initiates, Reviews and approves documentation that supports project execution andLead and execute Medium/Small-scale CI projects from initiation through closure.Track project milestones, deliverables, and KPIs to ensure timely completion.Collaborate with CI SMEs and operational teams to identify and implement processPrepare and present project updates to stakeholders and leadership.Support large-scale FFIP projects in conjunction with PMS (Portfolio Management Strategy)Assist in developing project charters, risk assessments, and communication plans.Monitor progress and escalate issues to project leads and FFIP leadership as needed.Acts as a key interface for technical transfers, and other major initiatives. Offers hands-onEnsure alignment with GMP, safety, and quality standards throughout project execution.Maintain project documentation and contribute to lessons learned and continuous.About YouBasic QualificationsBachelor's Degree is required.2+ years of experience in Continuous Improvement, Project Management or Engineering or related field in a cGMP-compliant pharmaceutical/ biotech, medical device, food industry environment, or an equivalent regulated setting.Required 100% on-site presence during regular workdays, with occasional support during off-shift hours, either remotely or on-site.Must have excellent written and verbal communication skills, as well as the ability actively, and cooperatively work with cross functional teams.Preferred SkillsMaster's Degree is preferred.Good team player with a collaborative mindsetFamiliarity with Qualipso Applications, including Change Control, CAPA, and Deviation management.Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scaleTransform lives worldwide by delivering life-changing treatments anywhere, anytime.Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.#GD-SP#vhdAll compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.