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 this new member to our growing QC team and company. This is both a strategic and people manager role. If you are a strong problem-solver, have an attention to detail, and enjoy cross-functional partnerships, this is the role for you! As the Manager, QC-Technical Services, you will work on various projects including:
Oversee Quality Control activities method transfer and validation efforts from early to late phase clinical products in compliance with ICH guidelines
Share expertise and troubleshoot a variety of analytical and bioanalytical techniques based on your extensive experience.
Manage a team to support external vendors projects, internal testing, and documentation related to contract organizations.
Author and critique internal and external document as well as regulatory submissions.
Build a rapport with internal stakeholders including Analytical Development, Quality Assurance, Regulatory Affairs, Technical Operations, and others.
If you have a bachelor’s or graduate degree in chemistry or life sciences, with a minimum 10 years of relevant biopharmaceutical industry experience in Quality Control, this may be the job for you! Ideally, you will have prior experience managing people. Expertise with method validation across all phases of clinical development is required as well as experience with regulatory health authorities (e.g. FDA, EMA). Excellent written and verbal communication skills are essential. You will have strong leadership qualities including strategic thinking, innovation, mentoring and collaboration.
Meet Your Future Team:
The Quality Control team is a self-motivated and lively group, with an innate curiosity to learn. You will report to the Associate Director, Quality Control. The QC Technical Service group within QC and will provides support to the QC Operations through ensuring analytical methods are ready to support GMP product throughout the product life cycle. This newly formed group will work closely with the Analytical Development and be part of the larger Quality team, currently made up for 15 individuals (and growing!).
The team is currently working virtually. While we do have plans to return into the Cambridge MA office, tentatively we are scheduled to return in June 2021. Although in a virtual environment, Intellia has made it a priority to continue to foster a sense of community. This includes virtual happy hours, team all hands, game nights, and more! You can expect to join a hardworking, collaborative environment. The team has led the charge and designed a robust virtual onboarding experience since the start of the pandemic.
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.