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Contract - Project Manager Consultant, Technology Transfer, MSAT

Kendall Square, Massachusetts, United States

About Be Biopharma

Be Biopharma (“Be Bio”) is pioneering Engineered B Cell Medicines (BCM) to dramatically improve patients’ lives who are living with cancer, rare diseases and other serious conditions. With eyes locked on the patient, our team of purpose-driven scientists, technologists, manufacturing experts and business builders collaborate to create a bold new class of cell therapies. Be Bio was founded in October 2020 by Longwood Fund and B cell engineering pioneers David Rawlings, M.D., and Richard James, Ph.D. from Seattle Children’s Research Institute. Be Bio is backed by ARCH Venture Partners, Atlas Venture, RA Capital Management, Alta Partners, Longwood Fund, Bristol Myers Squibb and Takeda Ventures. Since our founding, Be Bio’s investors have committed over $180 million to enable the Company to re-imagine medicine based on the power of B cell therapy. For more information, please visit us at Be.Bio and our LinkedIn page.

Culture

The beating heart of Be Bio is our People and together we are building a culture driven by purpose, passion, and that’s full of character.  We are “all-in” as we align ourselves with patients who need our medicines, and we embrace the highest standards of transparency, excellence, candor, collaboration, and team-based science with a shared ownership of company milestones and successes. 

Our commitment to our team members is to deliver a compelling, dynamic work experience that enables them to continually stretch, grow, and learn, that enriches their lives, that fosters a sense of belonging and community, and that goes above and beyond to support them in big, meaningful ways in both their personal and professional lives.  Be Bio is a team that works hard, plays hard, and supports each other on our shared journey to get transformative medicines to patients who need them. 

We are looking for a Project Manager Consultant to drive the coordination and execution of technology transfers to our CDMO partners. This role is about keeping the entire effort moving — aligning Development, MSAT, Quality, and Regulatory with our CDMO partners — and making sure timelines, deliverables, and risks are visible and managed. You’ll be the central organizer who ensures that the processes we develop in our labs get into the clinic on time. The role is hybrid; an ideal person would be on-site 2 to 3 days a week.

Responsibilities

  • Project planning and tracking: Own the overall project plans for tech transfers. Build and maintain integrated timelines across Manufacturing, MSAT, Development, Quality and Regulatory to ensure deliverables are completed on schedule.
  • Team leadership and coordination: Lead cross-functional transfer teams with clear agendas, documented decisions, and follow-up actions. Keep everyone aligned on scope, priorities, and responsibilities.
  • Stakeholder communication: Serve as the main point of contact between internal teams, stakeholders and CDMO transfer teams. Maintain transparent updates, risk registers, and escalation pathways for leadership.
  • Transfer Readiness: Partner with technical leads to coordinate transfer packages, protocols, and training materials. Ensure teams are prepared for engineering and GMP runs through a right-sized stage-gate process.
  • Issue and risk management: Track risks and decisions across the transfer. Coordinate resolution of issues with technical leads within project timelines.
  • Financial Oversight: Monitor project budgets and resource allocations in collaboration with finance and functional leads.
  • Continuous improvement: Identify opportunities to improve how we plan, execute, and communicate around tech transfers. Drive process improvements that enhance speed and reliability.
  • Be Awesome: Exhibit a positive attitude and a proactive approach to problem-solving, embracing challenges with enthusiasm and a solutions-oriented mindset.

Minimum Experience, Education, and Specialized Knowledge and Skills:

Must thrive in a fast-paced, growing, and innovative environment where flexibility, resourcefulness, resiliency, and communication skills are key. Excellent interpersonal and communication skills, ability to develop important relationships with colleagues, and being an all around good company citizen are essential.

  • Bachelor’s or Master’s degree in Life Sciences, Engineering, or related field.
  • 3-5 years of experience in biotech/pharma project management, ideally supporting early-phase cell or gene therapy programs.
  • Experience leading complex, cross-functional projects in a regulated setting.
  • Familiarity with cGMP manufacturing, technology transfer, or MSAT.
  • Strong organizational skills and proficiency with project management tools (MS Project, Smartsheet, etc.).
  • Excellent communication skills, with the ability to engage both technical and non-technical stakeholders.
  • Ability to manage competing priorities in a fast-paced environment.

Preferred Skills

  • 5+ years of experience in biotech/pharma project management, supporting early-phase cell or gene therapy programs
  • PMP Certification or Equivalent Training
  • Experience working with CDMO partners and external vendors
  • Familiarity with regulatory expectations for early-phase submissions

 

At Be Bio, we recognize that our people are our most valuable resources, and we are committed to offering a competitive rate. The anticipated hourly pay range for this role is $50.00/hr - $60.00/hr, effective for the current calendar year and is subject to market changes. Final rate will be determined based on a range of considerations, including—but not limited to—location, experience, skills, and alignment with role responsibilities.

 

 

 

 

 

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