Why Join Intellia?
Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.
Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.
We want all of our people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.
How you will Achieve More with Intellia:
We are excited to welcome a new member to our growing QC team and company. In this role you will drive activities related to testing performed internally and at contract organizations. You will manage a team to support externally sourced projects, internal testing, quality events, and documentation related to the assigned contract organizations. If you are organized, communicate well and have a strong attention to detail, this is the role for you. The individual will act as interdepartmental liaison to various groups, including Analytical Development, Manufacturing, and Quality Assurance. As the QC Manager you will be focused on our LNP and small molecule products, while working on various projects including:
- Manage product release testing activities at CMOs and contract labs to ensure the highest quality data is on time to support our clinical trials. This includes programs such as raw materials and reference standards.
- Improve systems and prevent problems using change controls and CAPAs. If issues do arise, you will make real time decisions to resolve in a GMP-compliant manner.
- Coach and mentor staff in all aspects of their job performance and career development.
- Maintain an ever-ready state of compliance.
You will have a minimum of Bachelor’s degree in a scientific field with 8+ years of experience in a GMP laboratory, and 5+ years of team leadership experience. Experience managing vendors is key.Strong technical understanding of analytical techniques, including HPLC/UPLC, CE, compendial, UV, bioassay and gel electrophoresis.Experience with LNP and/or Drug Products is ideal.Experience with electronic Quality systems (e.g. LIMS, EDMS).Knowledge with the interpretation and application of guidance’s including ICH, USP/NF, EP.
Meet your future team:
The Quality Control team is a self-motivated and lively group, with an innate curiosity to learn. The QC department supports release and stability testing for GMP products throughout the product life cycle. This QC role interacts with QC and QA on a daily basis as part of the expanding Quality team. We are moving to a hybrid working model, by working at home and together in our Cambridge offices.
Covid-19 Vaccination Policy: Effective Monday, January 3, 2022, all Intellia employees, regardless of work location, must be fully vaccinated for COVID-19. Requests for exemption for medical or sincerely held religious beliefs will be considered.
EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.