Development Associate II / Senior Development Associate

Full Time
San Diego, CA 92121
Posted
Job description

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!

We are looking to add a Development Associate II / Senior Development Associate to our Research and Development Team. The DA II / Sr. DA is responsible for following procedures, generating and documenting laboratory data, and drafting protocols, under supervision, in compliance with the IVS Quality Management.

Core Responsibilities Include:

  • Performs experiments and generates data in support of product development projects, under supervision.
  • 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, with supervision using available software.
  • Under supervision will begin to design experiments and write protocols (per standard guidelines).

You Bring:

  • BS degree in Molecular Biology or scientifically related field and 2+ year(s) of industry experience in a regulated environment preferred; equivalent combination may be considered.
  • 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) and the ability to learn new software programs.
  • Evidence of Covid-19 vaccination

We Bring:

  • 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.

Invivoscribe is an Equal Opportunity Employer.

Evidence of COVID-19 vaccination will be required as a condition of employment.

Job Type: Full-time

Pay: $70,000.00 - $94,000.00 per year

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Referral program
  • Vision insurance

Schedule:

  • 8 hour shift
  • Monday to Friday

Work Location: One location

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