Analytical Scientist
Analytical Scientist
Posted on :
14-11-2024
Employer Active
1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
14-11-2024
Job Description
Company Summary: 20bloc Inc is an earlystage biopharma company creating
breakthrough proteinbased drugs to save lives. We are developing a safe and effective hemoglobinbased 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 handson.
Position Overview: We are seeking a highly experienced laboratory scientist with a strong
conceptual understanding of and demonstrated expertise in analytical methods and Quality
Assurance functions in the area of biotherapeutics to support the daytoday operation of the
process development and production labs. This is an exciting opportunity to join a growing
expanding startup in a fulltime position on site in Thousand Oaks CA. We want a gogetter
who is curious takes initiative and learns quickly. If this is you we want to hear from you.
Key responsibilities:
Develop validate and optimize analytical methods to ensure accurate and reliable results
specific to our proteinbased products.
Conduct assays under defined protocols to measure purity potency and stability using
equipment and instruments supporting biotherapeutics.
Execute ELISA gel electrophoresis and chromatographicbased assays and qualification
activities following protocols on inprocess and final drug substance and drug product samples.
Write SOPs analytical protocols and written reports in compliance to cGMP as needed.
Routine lab activities as needed.
Requirements
Bachelor s degree in biological science or related field. Master s degree or higher preferred.
Minimum 510 years experience working in a laboratory with handson experience in
analytical method development assays and qualification activities.
Knowledge of GMPs SOPs and analytical processes within regulated laboratories.
Experience with accreditation and/or inspection processes is a strong plus.
Working knowledge of and exposure to phase appropriate quality systems including
deviations CAPA change control and document management systems.
Handson experience with protein analytical methods both compendial and noncompendial
such as HPLC (SEC AEX/CEX HIC RP etc.) and additional productspecific methods such
as ELISAs electrophoretic methods (SDSPAGE icIEF) endotoxin osmolality pH and
appearance strongly preferred. Experience with LCMS analyses and potency assay
development and execution a strong plus.
Experience with PCR western blot and MSbased methods a strong plus.
Excellent interpersonal verbal and written communication skills and the ability to work crossfunctionally such as with process development are essential in this collaborative work
environment.
Strong attention to detail and excellent organizational skills are required.
Benefits
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
Bachelor s degree in biological science or related field. Master s degree or higher preferred. Minimum 5-10 years experience working in a laboratory with hands-on experience in analytical method development, assays and qualification activities. Knowledge of GMPs, SOPs and analytical processes within regulated laboratories. Experience with accreditation and/or inspection processes is a strong plus. Working knowledge of and exposure to phase appropriate quality systems, including deviations, CAPA, change control, and document management systems. Hands-on experience with protein analytical methods, both compendial and non-compendial, such as HPLC (SEC, AEX/CEX, HIC, RP, etc.) and additional product-specific methods such as ELISAs, electrophoretic methods (SDS-PAGE, icIEF), endotoxin, osmolality, pH and appearance strongly preferred. Experience with LC-MS analyses and potency assay development and execution a strong plus. Experience with PCR, western blot and MS-based methods a strong plus. Excellent interpersonal, verbal and written communication skills and the ability to work crossfunctionally such as with process development, are essential in this collaborative work environment. Strong attention to detail and excellent organizational skills are required.
Employment Type
Full Time
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