Job: Biopharmaceuticas Analyst – Carlsbad

Title Biopharmaceuticas Analyst – Carlsbad
Categories California
Salary Up to $64K annually
Location Carlsbad, CA
Job Information

Opportunity

Our Fortune 500 client is seeking a Life Sciences graduate to join their team in Carlsbad, CA as a Process Development Analyst responsible for executing client and internal projects. As part of a dynamic organization, the successful candidate will work with Process Development team members to develop viral vector processes (upstream and downstream), execute process characterization studies, and develop and execute analytical testing.

Why Work Here

  • One of the top three R&D investors in the life science tools industry
  • Products and services for the biotech and pharmaceutical industries
  • Colleagues and challenges to unleash your innovative potential
  • Helping to advance the promise of life science

Responsibilities

  • Assist with planning, design, and execution of process development experiments for client projects and work with the Technology Transfer team to move these projects into Manufacturing
  • Support drafting process development worksheets and summary reports
  • Maintain mammalian adherent and suspension cell lines used for viral vector manufacturing
  • Develop and optimize downstream column chromatography processes
  • Assist with bench and pilot scale virus production using CellStacks and single use bioreactors
  • Assist with internal projects to develop and optimize unit operations for viral vector manufacturing
  • Assist with development and execution of analytical testing methods to measure process recovery, final viral titer, and impurity levels
  • Assist with lab maintenance and material ordering
  • Communicate effectively with cross-functional teams including Technology Transfer, Manufacturing, and other internal and external network partners

Qualifications

  • Bachelor’s Degree in Biochemistry, Biology, Chemistry, Chemical Engineering (Master’s a plus)
  • 1+ year of process development, engineering and/or manufacturing experience in the life science industry
  • Experience with large molecule biopharmaceutical production, viral vector production, mammalian cell culture processes (adherent and suspension), and single use systems
  • Experience with analytical test methodology, including qPCR, ddPCR, ELISA, HPLC
  • Experience with cell culture and aseptic technique
  • Large molecule / viral purification experience using chromatographic techniques
  • Knowledge or experience developing processes to transfer into clinical manufacturing
  • Ability to perform statistical analysis (JMP) and familiarity with design of experiments (DOE) studies

Benefits

  • Pay range is $60K to $64K W2 annually ($30 to $32 per hour), commensurate with experience
  • Optional participation in benefit plans (medical, dental, vision, disability, 401K)
  • Contract opportunity with potential for extension or direct hire

Apply

If your skills match the requirements for this exciting opportunity, please send us your resume.

Apply Now
Contact

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Email
info@cyber-inc.com

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