Associate Director Supply Chain Quality Assurance
Apply Now

Associate Director Supply Chain Quality Assurance

King of Prussia, PA

The Center for Breakthrough Medicines is on track to be the largest single-site cell and gene therapy contract development and manufacturing organization in the world. Our comprehensive service offering accelerates speed to market through supply chain disruption mitigation strategies, end-to-end program management expertise and unique platform technology with the ability to follow a molecule from idea to commercialization. CBM’s integrated approach provides high quality and consistent end-to-end manufacturing capability including: Process and Analytical Development; Plasmid DNA production; Viral Vector Production of Lentivirus; AAV and Adenovirus; Testing and Analytics; Autologous, Allogeneic and Gene-edited Cell Therapy Bioprocessing; and Cell banking. CBM’s horizontal and vertical integration provides one source throughout a product’s life cycle.

CBM’s mission is to accelerate the delivery and affordability of lifesaving and life-changing therapies from discovery to market by offering a complete solution for the development and commercialization of cell and gene therapies.


Center for Breakthrough Medicines seeks an intrinsically motivated quality professional with a growth mindset who will meet and exceed deadlines and quality expectations.

This role will be accountable to provide quality oversight on compliance and Good Manufacturing Practice (GMP) that pertains to the end-to-end Supply Chain activities to meet CBM’s standards and regulatory expectations.  These include quality oversight of materials management including receipt, storage, release, distribution, logistics, supplier complaints and internal investigations. 

The role will provide timely decisions and consultations in alignment with cGMP, CBM and regulatory guidelines.


  • QA oversight to the CBM Supply Chain end-to end materials management program, including processing of supplier complaints, material receipt and release, inventory control, shipping, and distribution. 
  • Escalate to Quality Management any quality and business risk(s) to CBM posed by materials suppliers.
  • Monitor and communicate supplier performance
  • Manage supplier changes and impact evaluation to CBM 
  • Conduct, execute and document thorough investigations and CAPAs. Ensure timeliness of deliverables through proactive intervention. May own CAPA action items or deliverables.
  • Maintain metrics
  • Support management reviews and other presentations
  • Maintain knowledge of regulatory environments, cGMPs, FDA policies and current industry trends and prepare and present written and verbal reports to upper management
  • Engage in cross functional organization to develop policies and processes to comply with new cGMP, USP, and CFR requirements/guidance at the site
  • Implement safety, quality and compliance improvement programs and initiatives. Innovate solutions to minor quality system gaps and participate in continuous improvement projects.
  • Troubleshoot quality/compliance issues, using experience, ingenuity, and creativity to provide solutions to a wide range of root causes
  • Supports assessment and documentation of issues that might pose compliance risks, supporting investigation and solutions, and actions.
  • Responsible for revising established processes and procedures which may impact multiple functions or regions.
  • Performs other duties, as assigned

Education & Experience

  • Bachelor’s Degree or higher
  • 7+years of experience in cGMP supplier and materials management, preferably in a quality assurance role
  • Strong knowledge of cGMP inventory management systems, particularly SAP. 
  • Strong collaborator, internally and externally, with exceptional time management and organizational skills
  • Proven manager, mentor, and team developer, with the ability and desire to grow an organization, and facilitate the dynamics of growth and achieving goals
  • Excellent written and verbal communication skills
  • Excellent analytical, prioritization, multi-tasking, communication, and strong leadership skills and the ability to work independently without supervision
  • Prior experience preparing and presenting written and verbal reports to upper management and business unit heads
  • Successfully drive projects forward to meet program/project deliverables
  • Excellent judgment and creative problem-solving skills, including negotiation and conflict resolution skills
  • Ability to work effectively on cross functional teams
  • Strong influencing skills

Compensation: TBD

Apply Now