Upstream Process Scientist - Ambr250 (Weekends)

EurofinsMalvern, PA
15dOnsite

About The Position

Perform Upstream process development utilizing the Ambr250 Satorius system for large molecule based products within the API-Proteins group Perform duties in a protocol-driven work, such as cell culture, and running Ambr bioreactors Supporting lab work associated with development and scale-up projects within the API-Proteins area Responsible for organizing records, capturing results into data sheets, and contributing to technical reports in a team environment as well as contributing individually to meet project timeline and objectives Assist with general lab upkeep and organization efforts, which includes decontamination and disposal of large-scale cell culture/bioreactor wastes Conduct, analysis and reporting of data in accordance with requirements set forth by the department Record experimental data and accurate and highly organized laboratory notebooks Comply with cGMP practices Analyze and present data in professional format Demonstrate clear and professional verbal and written communication. Follow appropriate SOPs and all internal documentation requirements We are considering this role for either a Tuesday-Saturday or Sunday-Thursday 9:00am-5:00pm shift.

Requirements

  • Bachelors or Master’s degree in biopharmaceutical, biotechnology or pharmaceutical required
  • Broad knowledge in upstream process development and hands-on experience
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Responsibilities

  • Perform Upstream process development utilizing the Ambr250 Satorius system for large molecule based products within the API-Proteins group
  • Perform duties in a protocol-driven work, such as cell culture, and running Ambr bioreactors
  • Supporting lab work associated with development and scale-up projects within the API-Proteins area
  • Responsible for organizing records, capturing results into data sheets, and contributing to technical reports in a team environment as well as contributing individually to meet project timeline and objectives
  • Assist with general lab upkeep and organization efforts, which includes decontamination and disposal of large-scale cell culture/bioreactor wastes
  • Conduct, analysis and reporting of data in accordance with requirements set forth by the department
  • Record experimental data and accurate and highly organized laboratory notebooks
  • Comply with cGMP practices
  • Analyze and present data in professional format
  • Demonstrate clear and professional verbal and written communication.
  • Follow appropriate SOPs and all internal documentation requirements

Benefits

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
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