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Scientist II (ELISA, Cell Based Potency Assays)
Scientist II (ELISA, Cell Based Potency Assays)The Fountain Group • Irvine, CA, United States
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Scientist II (ELISA, Cell Based Potency Assays)

Scientist II (ELISA, Cell Based Potency Assays)

The Fountain Group • Irvine, CA, United States
6 days ago
Job type
  • Full-time
Job description

100% ONSITE IRVINE CA

Pay : $47-$52 / hr

Contract : 1 year

REQUIRED : qELISA

Cell-Based Potency Assays

dose response curves

Cell Culture

Biology

Job Description :

The Scientist is responsible for supporting the development, qualification, transfer, and validation of analytical methods with experience required in the following :

  • Cell-based potency assay / bioassay and quantitative ELISA (qELISA).

He / She collaborates with scientific staffs to plan experimental work and executes protocols in support of biologics process development, formulation development, and stability studies. The individual independently generates, compiles, and evaluates data for technical reports to support regulatory filings for new and currently marketed biological products. The individual is also responsible for writing sections or subsections of technical reports, method and / or operational SOPs. He / She independently carries out multiple analytical methods to support Client biologics projects depending on departmental needs. Maintains a productive and collaborative laboratory environment consistent with regulatory and company expectations.

The position requires the individual to work with and in areas requiring select agents and toxins access (i.e. Biosafety level 2 laboratories). Access to and use of select agents is regulated by federal policies. Therefore, the candidate must conduct all work activities in compliance with Client internal and applicable regulatory requirements. Client internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives.

  • Support development of phase appropriate separation methods to support toxin development programs
  • Execute the development and validation of analytical methods for the analysis and characterization of biopharmaceuticals. Create written procedures and protocols. Transfer, qualify or validate methods as needed.
  • Apply routine and specialized analytical techniques to characterize and quantify biopharmaceuticals. Maintain reagent supplies, notebooks, summarizes results in written reports and communicates observations to ensure that the end user receives quality methods in a timely manner. Comply with Quality Principals related to data generation and reporting.
  • Actively participate on cross-functional teams within Biologics Development and provide support to external departments. Openly share scientific expertise and collaboratively help the team to formulate rational solutions to problems.
  • Develop protocols and SOPs, train staff and maintain the laboratory consistent with departmental and company requirements. Understand, document, and adjust Quality Systems to match the project stage (e.g. pre-development or development).
  • Maintain a good and current knowledge of the scientific and technical literature pertinent to the project and necessary for development of state-of-the-art analytical methods, including the acquisition of necessary equipment.
  • Make high quality scientific presentations at internal management, regional and national meetings to help advance Client's image as the thought and product leader in the neuromodulator field. Present and defends product, assay and process data to regulatory agencies.
  • Qualifications

  • Bachelor's Degree or equivalent education with at least 2 years of experience, or Master's Degree or equivalent education with typically 0 - 4 years of experience.
  • Experience in the area of developing and qualifying in vitro cell-based assays to reflect the relevant molecular mode of action.
  • Experience in cell culture and state-of-the-art cell and molecular biology, immunoassay, and bioassay techniques.
  • Knowledge and experience in developing, validating, and transferring separation methods for biologics, including qELISA (quantitative), Cell-Based Potency Assays (CBPA), enzyme activity / functional assays and other bioassays.
  • Understanding of methods and procedures related to the production and characterization of biopharmaceuticals in a regulated environment is expected.
  • General understanding in CMC development strategy of biologics drugs is expected.
  • Understanding of how neurotoxin structure relates to biological function is a plus.
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