ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential.
The Role:
ElevateBio is looking for a Sr. Quality Engineer to provide QA oversight and strategy for the BaseCamp technology transfer. In this role the Sr. Quality Engineer will be responsible for managing cGMP compliance from a Quality Assurance perspective of technology transfer activities including process characterization, PPQ and Engineering manufacturing runs. In addition, this position with support all process and technology transfer risk assessments, technical reports, change controls, deviations and CAPAs related to process validation and technology transfer activities. The candidate will contribute to team based collaborative environment promoting commitment to continuous improvement and achievement of goals within the QA group.
Here’s What You’ll Do:
- Provide QA oversight of engineering run and process performance qualification protocols, reports, and discrepancies.
- Provide QA oversight in the development, review, and execution of technical protocols, reports, risk assessments, and discrepancy management.
- Provide QA oversight for Process Characterization activities.
- Provide QA oversight and expertise for clients transitioning from clinical to commercial manufacturing.
- Change control assessment and approval to assure proper impact assessment and sufficient testing to develop and maintain a validated state.
- Review and assist in investigating deviations and discrepancies related to process validation testing and technology transfer activities.
- Manage/complete Quality Risk Assessments (QRA) for Process Validation and Technology Transfer activities.
Requirements:
- Bachelor’s Degree in engineering, life sciences or related field with 10+ years of quality experience.
- Prior experience in Cell and Gene Therapy manufacturing preferred.
- Strong knowledge in technology transfer. Process validation and process characterization preferred.
- Experience in working in a Contract Manufacturing environment preferred.
- Technical proficiency & knowledge in use of enterprise electronic data management and execution systems (i.e. ERP, QMS, DMS, and MES) preferred.
- Strong technical writing skills and proficiency in various computer programs (Word, Excel, PowerPoint).
- A collaborator who communicates in an open, clear, complete, timely and consistent manner.
Why Join ElevateBio?
ElevateBio is a technology-driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry-leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
We aim to be the dominant engine inside the world’s greatest scientific advancements harnessing human cells and genes to alter disease.
Our Mission:
To power the creation of life-transforming cell and gene therapies, at a speed the world deserves.
Our Vision:
We seek to be the world’s most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
What We Do
ElevateBio is a technology driven company powering transformative cell and gene therapies today and for many decades to come.
The company has assembled industry-leading talent, built world-class facilities, and integrated diverse technology platforms necessary for rapid innovation and commercialization of cell, gene, and regenerative therapies. The company has built an initial technology stack, including gene editing, induced pluripotent stem cells, and protein, viral, and cellular engineering. At the center of the business model is ElevateBio BaseCamp, a centralized R&D and manufacturing company that offers research and development (R&D), process development (PD), and Current Good Manufacturing Practice (CGMP) manufacturing capabilities. The company is focused on increasing long-term collaborations with industry partners while also continuing to develop its own highly innovative cell and gene therapies. ElevateBio's team of scientists, drug developers, and company builders are redefining what it means to be a technology company in the world of drug development, blurring the line between technology and healthcare.
ElevateBio is headquartered in Cambridge, Mass, with ElevateBio BaseCamp located in Waltham, Mass.
