Codetta Bio Inc. is a venture-backed life sciences company with innovative solutions to some of the most significant challenges in the life sciences and healthcare industries. We are developing advanced multi-omic biomarker measurement tools supporting data-driven approaches to understanding the unique genetic, environmental, lifestyle, and clinical factors that contribute to individual health and wellness. Guided by an experienced leadership team, Codetta offers a high-energy, collaborative work environment with opportunities for professional advancement.

The ideal candidate will be self-motivated, organized with excellent laboratory skills and good communication skills. The candidate must be comfortable in a fast-paced environment where everyone holds each other accountable.

Major Responsibilities:

• Perform research and tests in support of product development and validation

• Work both independently and on a cross-functional team in a fast-paced, deadline-driven environment

• Work under senior staff to develop/test assays, kits, and reagents

• Work within appropriate regulatory framework (GLP, GMP) where required

• Maintain organized electronic and paper records of experimental conditions and results

• Generate reports using provided data analysis software and templates

• Assure that work is completed in a timely fashion

• Work within a Biosafety Class 2 laboratory, following appropriate protocols and procedures

• Identify and troubleshoot potential problems with the help of senior staff

• Present data at regular meetings and contribute to scientific publications

• Occasional evening or weekend work when required

Required Qualifications:

• Education: Bachelor’s or master's in biology, biochemistry, bioanalytical chemistry, chemistry, molecular biology or related discipline

• Experience: Bachelor’s degree with 1+ years of experience

• Adept at handling DNA, RNA, and biological/clinical samples with aseptic technique

• Experience with standard life science techniques including RT-PCR, DNA/RNA extraction, and immunoassays / ELISAs

• Comfortable working with iterations of prototype devices and assay protocols

• A curious disposition, a drive to learn scientific principles and techniques and creatively apply them to develop novel, impactful products

• Excellent oral and written communication skills

Preferred Qualifications:

• 3+ years of industry experience

• Understanding of Design Controls and history of working in an FDA-regulated environment and/or in accordance with GLP

Work Location: Morrisville, NC. On-site laboratory