Scientist, Analytical Development

Location
Cambridge, MA, United States
Posted
Dec 02, 2020
Ref
1583761532
Hotbed
Genetown
Required Education
Doctorate/PHD/MD
Position Type
Full time
Our mission:

Developing curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.

At Intellia, we are committed to solving the complex challenges of making CRISPR/Cas9-based medicines a reality for patients suffering from genetic diseases and to create novel engineered cell therapies for immuno-oncological and autoimmune diseases.

Intellia is seeking a motivated Analytical Development candidate for a position as Bioassay Scientist to work on our gene and cell therapy clinical programs. The candidate must have a strong background and hands-on experience in molecular and binding/immunoassays. The successful candidate will take a leading role in defining, developing and optimizing new methods, as well as facilitating method transfers, qualifications and validations. He/She will be responsible for analytical development, qualification, and operational support for preclinical through late stage clinical development programs for Intellia Therapeutics.

Responsibilities:
    • Develop, optimize, and qualify molecular-based, immunoassay, and characterization assays with established assay acceptance criteria for gene & cell therapy product characterization, lot release and stability testing
    • Technology Transfer: Act as SME in tech transfer of analytical methods, protocols/procedures, and know-how from internal labs to external labs
    • Lab operation: Routine and non-routine analytical testing, coordination with internal/external PD or cGMP manufacturing on sample testing, maintain laboratory equipment, maintain laboratory sample inventory for potency assay, compile and present data to support process development and developmental stability studies
    • Evaluate novel assay technologies and methodologies that could improve existing analytical methods
    • Knowledge of GxP regulations
    • Author and review SOPs, development reports, and assist in the preparation of CMC regulatory submissions
    • Assist in maintaining/qualification of critical reagent supply for assigned methods
    • Work collaboratively with Analytical Development, Process Development and Quality teams to gather and analyze data to achieve method readiness
    • Work closely with, and support quality control on investigations, OOS, OOTs and release assay trouble shooting
    • Maintain well documented records of analytical data, laboratory notebooks, execution of assays and stability data


Qualifications:
    • PhD degree in Biochemistry, Cell & Molecular biology, Genetics, or related disciplines with minimum 2+ years of experience; Master's degree with minimum 5+ years of experience; BS with minimum 10+ years of experience in biotech or pharma industry with primary focus on biologics and/or gene and cell therapy
    • Excellent communication, technical and organizational skills are required
    • Managerial experience desirable
    • Critical thinking, troubleshooting and attention to detail is a must. Candidate will be required to plan & execute experiments as well as analyze data generated at other sites for method improvements
    • AAV and/or Cell Therapy experience is highly desired
    • In depth knowledge of molecular assays such as qPCR, ddPCR and/or ELISA and enzymatic assays experience is required
    • Prior experience or technical knowledge in NGS is desirable
    • Knowledge of FDA, cGMP, and ICH regulatory requirements in the context of bioassay/potency assay development and qualification is desired
    • Experience and knowledge of QC and GMP regulations is essential
    • Extensive experience in cell culture, cell line development is required
    • Must be able generate SOPs and technical reports with appropriate level of detail, as well as perform bioassay assay trending
    • Must have experience working with CROs
    • Good understanding of statistical methods/tools for data analysis is strong plus
    • Team player, good interpersonal and organizational skills


#LI-KO1

What Intellia Stands For:

We push boundaries. We are focused on positively disrupting health care treatment of patients with genomic diseases. The values we live by and drivers we look for are:

- One is respect for individuals; our unique qualities and strengths; our own ways to understand, learn and improve. One is our single-minded determination to excel; to succeed together. One is you and us - trusting and counting on every single one of us.

- Explore because we seek new ways to tackle disease. Explore with unbounded minds...free from assumptions, open to ideas. Explore by staying curious, by pushing boundaries, overcoming obstacles. Explore means thinking of new ways.

- Disrupt by thinking courageously...and creating a better future. Disrupt by defying conformity; interrogating the status quo; questioning our momentum. Disrupt with challenging thoughts...with that breed of skepticism that shows you have better solutions.

- Deliver with your focus on the objective and your determination to complete the task. Deliver by advancing relentlessly and by maintaining high standards...even when nobody is watching. Deliver by staying accountable and pulling your weight. Deliver because patients are counting on us to make the promise reality. Get it done.

POSITION: Full-Time, Exempt

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.

Intellia's web-based application process is managed through Lever. Information submitted through application forms is collected by Lever and subject to Lever's privacy policy .