Project Manager

Overview Team is seeking a highly motivated Contract Project Manager to support the planning, execution, and delivery of strategic projects across cell therapy manufacturing operations. This role focuses on driving initiatives related to technology transfers, process validation, raw material qualification, new product launches, and technical operations excellence. The Contract Project Manager will work closely with cross-functional teams within MSAT, manufacturing, quality, supply chain, IT, and external partners to enable timely and quality execution of site and global projects. Key Responsibilities Lead planning and execution of assigned technical operations/MSAT projects (e.g., tech transfer, process validation, new facility readiness). Develop detailed project schedules, Gantt charts, and integrated timelines to support project tracking and scenario planning. Organize and facilitate project meetings; document meeting minutes, action items, and key decisions. Track, manage, and communicate project risks, issues, and mitigation strategies; maintain and update risk registers. Support change management activities and ensure alignment with cGMP and regulatory requirements. Prepare and deliver project status reports and presentations to stakeholders, project sponsors, and leadership. Coordinate operational handoffs and project closure activities. Cross-functional Collaboration – Identify and engage stakeholders, drive alignment on project requirements, scope, and deliverables. Collaborate with matrixed teams (quality, supply chain, IT, MSAT, manufacturing, etc.) to ensure smooth project execution. Assist with resource planning and allocation in OnePlan, including supporting budget management and capital request processes. Tools & Process Improvement – Apply and promote best practices in project management, leveraging PMO methodologies and tools (OnePlan, MS Project, Smartsheet, Tableau, SharePoint). Champion excellence in documentation, data-driven decision-making, and continuous process improvement within technical operations. Qualifications & Experience Required Bachelor?s degree in engineering, life sciences, or related discipline. Master?s degree preferred. Minimum 5 years of relevant experience in project management in biotech, pharmaceutical, or cell therapy manufacturing environment; MSAT experience highly desirable. Demonstrated experience leading cross-functional projects in regulated (FDA/cGMP) environments. Proficient in project management and collaboration tools (MS Project, Smartsheet, Tableau, SharePoint, Excel, PowerPoint). Strong organizational, analytical, and problem-solving skills; proven ability to manage multiple complex projects simultaneously. Exceptional verbal, written, and presentation skills. Self-starter, able to drive projects independently and thrive in dynamic, fast-paced settings. PMP or CAPM certification strongly preferred. Experience in business process improvement and change management is a plus. Work Arrangement & Location 50% onsite Work Schedule: Mon-Fri (normal business hours) Work Location: Devens, MA or Giralda, NJ Contract & About ASK Consulting This posting is for a contract assignment with ASK Staffing DBA ASK Consulting to provide services to Bristol Myers-Squibb . Compensation: The starting hourly compensation range is $48 - $52.45/hr . Final compensation and benefits are determined by the employer of record. Benefits & Equal Opportunity ASK Consulting provides comprehensive, ACA-compliant health coverage, along with dental, vision, Short- and Long-Term disability for eligible employees. We also offer commuter benefits, a 401(k) plan with no matching, and a referral bonus program. In addition, ASK Consulting offers unpaid leave and paid sick leave as required by law. Equal Opportunity Employer: ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws. California Applicant Notice: ASK Consulting is committed to complying with the California Privacy Rights Act (CPRA), effective January 1, 2023, as well as all relevant data privacy laws. Applicants may review our Notice to California Job Applicants Regarding the Collection of Personal Information and may request this notice in an alternative format by contacting View email address on click.appcast.io. Fair Chance Employment Notice: If selected for a position at ASK Consulting, the offer is contingent upon several requirements, which may include a criminal background check. We consider qualified applicants with arrest or conviction records in accordance with applicable laws. The background check will evaluate whether any criminal history could pose a direct, negative impact on job-related safety, security, trust, regulatory compliance, or overall suitability for the role. Findings that raise concerns may result in withdrawal of a conditional job offer. Privacy: This posting does not constitute an offer of employment. All applicants must be legally authorized to work in the United States. Any eventual offer of employment will be at-will, regardless of assignment duration. #J-18808-Ljbffr Bristol Myers Squibb