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Research Associate

2 months ago

thousand oaks, United States 20BLOC Full time

Who we are: 20bloc, Inc. (www.20bloc.com) is an early-stage biopharma company creating breakthrough protein-based drugs to save lives. We are developing a safe and effective hemoglobin-based oxygen carrier for first response, organ preservation and oxygen therapy. We value and encourage innovations through robust information exchange, hard work, and team interaction. We are collaborative, we are intellectual, we are hands-on.

 

Job Title: Research Associate (Analytical Development)


  • Position Overview: We are seeking an experienced laboratory scientist with a conceptual understanding of quality functions who is knowledgeable in analytical methods in the area of biotherapeutics to support the day-to-day operation of and liaise with the analytical testing labs. This is an exciting opportunity to join a growing, expanding start-up in a full-time position on site in Thousand Oaks, CA. We want a go-getter who is curious, takes initiative, and learns quickly. If this is you, we want to hear from you.

 

Key responsibilities:

  • Conduct assays under defined protocols with minimal supervision to measure purity, potency, and stability using equipment and instruments supporting biotherapeutics.
  • Develop, validate and optimize analytical methods to ensure accurate and reliable results specific to HBOC products.
  • Execute ELISA, gel electrophoresis and chromatographic-based assays and qualification activities following protocols on in-process and final drug substance and drug product samples.
  • Participate in drafting SOPs, running test methods, analytical protocols and written reports in compliance to cGMP as needed.
  • Perform routine lab activities as assigned.


Requirements:

  • Bachelor’s degree in biological science or related field. Master’s degree preferred.
  • Minimum 2+ years’ experience working in a laboratory with hands-on experience in assays and qualification activities.
  • Familiarity with GMPs, SOPs and analytical processes within regulated laboratories. Experience with accreditation and/or inspection processes is a strong plus.
  • Working knowledge of phase appropriate quality systems, including deviations, CAPA, change control, and document management systems.
  • Experience in HPLC methodologies and other applicable methods for the testing of biopharmaceuticals.
  • Experience with PCR, western blot and MS-based methods a strong plus.
  • Excellent interpersonal, verbal and written communication skills and the ability to work cross-functionally such as with process development, are essential in this collaborative work environment.
  • Strong attention to detail and excellent organizational skills are required.


This position provides an excellent opportunity for a highly motivated, collaborative individual to apply their skills and experience in an early-stage biopharma company with room for advancement while contributing to the development of a groundbreaking therapeutic protein product.


We offer a comprehensive benefits package which includes:

  • Medical, dental and vision plans
  • 120 hours paid time off (PTO)
  • 12 paid holidays annually
  • 401(k) U.S. retirement savings plan
  • Employee assistance program

20bloc is an equal opportunity employer and values diversity. We provide the same opportunities disregarding race, religion, color, national origin, gender, gender identification, sexual orientation, age, marital status, veteran status, or disability status.