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Senior Development Associate



Job Location

10222 Barnes Canyon Rd. Bldg 1
San Diego, CA 92121
United States


80k to 90k


A beautiful modern facility centrally located in San Diego County, with many jobs conducive to a hybrid work from home arrangement.
A safe, fully-vaccinated, work environment.
A diverse and inclusive work environment where you will learn, grow, and make new friends.
A well-stocked breakroom with hot and cold beverages, snacks, refrigerator and pantry items to get you through the day.
Competitive salaries and bonus program, incentive stock options, amazing benefit options, a 401k plan with a fully vested employer match, and generous time off benefits that include floating holidays.

Job Description

We are looking to add a Senior Development Associate to our Research & Development Team. The Senior Development Associate is responsible for independently designing, analyzing, and executing experiments and writing documents, with some supervision, in compliance with the IVS Quality Management System (QSR) and applicable regulations.

Core Responsibilities Include:

Independently performs experiments and generates data in support of product development projects.
Maintains a laboratory notebook (and electronic documents) that records all aspects of experimental design and results, following good documentation practices, at all times.
Responsible for accuracy and completeness of auditable documents.
Performs data analysis using available software with limited supervision.
Under supervision, designs experiments and writes protocols (per standard guidelines) and reports.
Reviews laboratory notebooks, experimental designs, and draft protocols and reports of peers for accuracy and compliance.


BS in Molecular Biology or scientifically related field with 5+ years of industry experience in a regulated environment; equivalent combination may be considered. Advanced degree advantageous.
Familiarity with quality and regulatory requirements in the following environments a plus: medical device, in vitro diagnostic, GLP, cGMP (QSR), IVDR or ISO.
Proficient computer skills and good working knowledge of Microsoft Office programs. (Word, Outlook, Excel and PowerPoint)
Evidence of Covid-19 vaccination.

About Our Organization

Invivoscribe is an industry pioneer in oncology diagnostics, dedicated to improving the standard of global healthcare for over 25 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used in over 160 countries. Our global network of laboratories offer next generation molecular and flow cytometry panels to support our drug development entity and accelerate clinical trials. Our harmonized clinical laboratories offer a menu focused on clinically significant biomarkers which support therapeutic decisions, minimal residual disease (MRD) monitoring, patient stratification, trial enrollment, and the development of companion diagnostics. For 25 years, we have stood at forefront of precision diagnostics, and we’re just getting started!