Senior Upstream Process Scientist – Mammalian (Temp)

AstraZeneca plc

Cambridge

On-site

GBP 60,000 - 85,000

Full time

4 days ago
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Job summary

AstraZeneca plc is seeking a Senior Scientist – Upstream Process Development for a temporary maternity-cover role in Cambridge. You will carry out hands-on mammalian cell culture process development, focusing on CHO systems, process optimization, and technology transfer to GMP facilities, while coordinating with cross-functional teams.

Responsibilities include experimental design, data analysis, and reports to support CMC and regulatory submissions.

Qualifications

  • Degree (BSc/MSc/PhD) in biochemical engineering, bioprocessing, biotechnology or related scientific discipline.
  • Sound knowledge of mammalian upstream process development, media/feed design and CHO culture.
  • Hands-on aseptic cell culture experience including cryopreservation and inoculum expansion.
  • Ability to plan, execute, analyze and report process-development studies independently.

Responsibilities

  • Deliver upstream process development activities across CMC development cycles under minimal supervision.
  • Design and interpret mammalian cell culture studies (CHO-based) including fed-batch and perfusion.
  • Operate high-throughput bench-scale bioreactors (AMBR, <10 L) and data-driven optimization.
  • Apply DoE and statistical analyses to identify process drivers and robustness.
  • Coordinate workload across multiple work packages and support tech transfer to GMP facilities.

Skills

Mammalian upstream process development
Aseptic cell culture
Design of Experiments
Data analysis and interpretation
Verbal presentations and written+

Education

BSc/MSc/PhD in biochemical engineering/bioprocessing/biotechnology

Tools

Bench-scale bioreactors
Ambr systems

Job description

AstraZeneca plc is seeking a Senior Scientist – Upstream Process Development for a temporary maternity-cover role in Cambridge. You will carry out hands-on mammalian cell culture process development, focusing on CHO systems, process optimization, and technology transfer to GMP facilities, while coordinating with cross-functional teams.

Responsibilities include experimental design, data analysis, and reports to support CMC and regulatory submissions.

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