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Associate Director Of Operations
Company | Legend Biotech |
Address | Raritan, NJ, United States |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology Research |
Expires | 2023-07-30 |
Posted at | 11 months ago |
Company Information
- Lead facility operating review meetings and own various department projects to drive continuous improvements and efficiencies within cell therapy Technical Operations.
- Build strong partnerships with Manufacturing, Engineering, and Quality to ensure seamless execution of daily production schedules.
- Oversee cell therapy production and ensure safe and compliant manufacturing operations according to cGMP requirements.
- The role will require proven leadership to drive effective communication, coordination, and collaboration across relevant cross functional groups to ensure robust production, testing and release of product to patients.
- Be responsible for multiple work centers within the facility to ensure high quality and compliant product supply and oversee production metrics.
- Support the operations organization build, operations ramp-up of commercial and clinical production.
- Oversee the hiring, development, and performance management of staff, and assign personnel to execute daily production schedules.
- Support manufacturing investigations, support, and manage change controls, and maintain permanent inspection readiness and actively support regulatory inspections.
- Excellent teamwork and interpersonal skills with ability to influence and build strong working relationships at all levels
- Clear and succinct verbal and written communication skills.
- Minimum of 5 years of experience in a leadership role in Biologics and/or cell therapy operations
- Experience with Operational Excellence and/or Lean Manufacturing is an asset.
- Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members.
- B.Sc./M.Sc. in Biological/Biochemical Science/Bioengineering or related field.
- Project management skills, responsiveness to issues, and demonstrated passion for creating new medicines.
- Communicates effectively with people at all levels, including the ability to understand their priorities, and to earn their respect and trust, along with the willingness to provide them with the best decisions in time-sensitive situations
- A history of developing and building cohesive, high performing teams with a strong sense of mission, providing training and mentoring to build sufficient management depth throughout the organization and ensure strong succession planning
- Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability.
- An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment.
- Minimally 8+ years of combined experience in cGMP manufacturing, operations management, tech transfer, process and equipment validation and quality management, with a preference for Cell/Gene Therapy experience
- Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively.
- Hospital Indemnity Insurance
- Short-Term Disability
- Employee Assistance Program
- Health Savings Account
- Matched 401K
- Flexible Spending Account
- Paid Maternity Leave
- Vision Insurance
- AD&D Insurance
- Legal Insurance
- Critical Illness Insurance
- Long-Term Disability
- Paid Paternity Leave
- Pet Insurance
- Dental Insurance
- Life Insurance
- Commuter Benefits
- Accident Insurance
- Health Insurance
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