Scientific Associate – Process Development & GMP

Pharmaron

Liverpool

On-site

GBP 32,000 - 42,000

Full time

13 hours ago
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Benefits offered by this job

Career development
Team environment
Growth opportunities

Job summary

Pharmaron is seeking a Scientific Associate to support studies in the Process Development laboratories or production batches. You will design, execute and report experiments to meet project timelines within GMP/compliant systems, under senior supervision.

We look for a BSc/MSc in a related field with at least 1 year of industry experience, familiarity with mammalian/microbial/viral processes, and strong collaboration to drive multi-disciplinary projects forward.

Qualifications

  • BSc/MSc in a related field or equivalent.
  • Minimum 1 year’s industry experience (post-grad employment or industrial placement).
  • Knowledge and prior experience of mammalian, microbial or viral processes or GMP.
  • Knowledge of Molecular Biology.
  • Evidence of ability to contribute to multi-disciplinary scientific teams.
  • Strong academic or industrial achievement.

Responsibilities

  • Support project leads on delivery of internal and client-based work packages.
  • Design, deliver and report experimental work to meet project timelines in line with development policies and procedures.
  • Maintain exemplary standards in the laboratory and facility in compliance with Development, Quality and EHS Policies.
  • Execute pilot plant or GMP manufacturing records and drive validation activities.
  • Drive activities in compliance with cGMP and Pharmaron quality systems.
  • Expand expertise related to GMP manufacture, upstream/downstream process development or cell line development.

Skills

Mammalian/microbial/viral processes
Molecular Biology
Multi-disciplinary teamwork

Education

BSc/MSc in related field

Job description

Pharmaron is seeking a Scientific Associate to support studies in the Process Development laboratories or production batches. You will design, execute and report experiments to meet project timelines within GMP/compliant systems, under senior supervision.

We look for a BSc/MSc in a related field with at least 1 year of industry experience, familiarity with mammalian/microbial/viral processes, and strong collaboration to drive multi-disciplinary projects forward.

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