QA Investigations Lead (2nd shift, Sun-Thurs)
QA Investigations Lead (2nd shift, Sun-Thurs)
Legend Biotech
Raritan, NJ
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Company Information
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK) cell-based immunotherapy.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a QA Investigations Lead (2nd or 3rd shift) as part of the Quality team based in Raritan, NJ.
Role Overview
The QA Investigations Lead has the responsibilities for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations, ownership of various department projects, and tracking of quality metrics while ensuring high quality and complaint product supply.
Key Responsibilities
Legend Biotech maintains a drug-free workplace.
Benefits:
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK) cell-based immunotherapy.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a QA Investigations Lead (2nd or 3rd shift) as part of the Quality team based in Raritan, NJ.
Role Overview
The QA Investigations Lead has the responsibilities for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations, ownership of various department projects, and tracking of quality metrics while ensuring high quality and complaint product supply.
Key Responsibilities
- Support compliance activities for site Quality Operations in accordance with Legend standards, procedures and cGMPs
- Collaborate with site personnel to provide guidance and determine resolution for manufacturing issues
- Ensure accurate and timely maintenance and review of manufacturing investigations, CAPAs, change controls and complaints
- Review and approve manufacturing procedures
- Support regulatory inspections and audits by ensuring inspection readiness within facility
- Perform internal housekeeping audits
- Perform analysis on quality indicating data and identifying trends
- Provide oversight for trending of quality compliance metrics
- Work in a collaborative team setting with quality counterparts that include Manufacturing Operations, Operations Technical Support, Maintenance, Supply Chain and Planning
- A minimum of a Bachelor’s Degree in Science, Engineering or equivalent technical discipline is required
- A minimum of 4 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy
- Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices
- Great attention to detail and ability to follow the procedures
- The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision
- Good written and verbal communication skills are required
- Ability to summarize and present results, and experience with team-based collaborations is a must
- Must be able to interpret problems and effectively determine appropriate resolutions that ensure compliance and minimize risk
- Must exhibit strong leadership skills and effectively develop others
- Ability to collaborate well with stakeholders, customers and peers
- Must exhibit strong decision-making ability and think creatively while maintaining compliance and quality
- Must be able to discern the criticality of issues and to communicate to management regarding complex issues
- Ability to manage conflict and issues that arise with internal or external customers
Legend Biotech maintains a drug-free workplace.
Benefits:
- Health Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
- Matched 401K
- Flexible Spending Account
- Health Savings Account
- AD&D Insurance
- Short-Term Disability
- Long-Term Disability
- Paid Maternity Leave
- Paid Paternity Leave
- Pet Insurance
- Critical Illness Insurance
- Hospital Indemnity Insurance
- Accident Insurance
- Legal Insurance
- Commuter Benefits
- Employee Assistance Program
-
Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Quality Assurance -
Industries
Biotechnology Research
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