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Principal Research Associate- Large Pharma



Business Type: Pharmaceutical Company
Job Type: Biotechnology, Quality Assurance - Control
Job Level: Experienced (non manager)
Position: Full Time
Location: USA - Massachusetts
Reference: GL310167.2
Closing Date: 31/01/22
Job Details:

Our client is a leading company in search of a driven Principal Research Scientist.

This candidate will participate in the development, qualification, and transfer of cell-based, binding and molecular methods used for analyzing cell & gene therapy candidates in clinical development, including cGMP release and stability testing of clinical trial material as well as critical raw materials.

We are looking for someone with an innovative mindset, excellent communication skills, and a proven ability to work with a high level of integrity, accuracy, and attention to detail.

Key Responsibilities:

  • Work under minimal supervision to develop and implement cell-based assays for potency and other parameters per ICH and regulatory guidelines
  • Perform cGMP sample testing by following method protocols (SOPs) and ensure timely completion and delivery of analytical results
  • Work within a broader team to evaluate and implement new technologies and ways of working to enable agility and innovation in the workflow.
  • Serve as a technical resource to solve analytical method and instrument issues
  • Work collaboratively with other teams within GMU s
  • Ensure timely completion and delivery of analytical results and documentation

Must haves:

  • Master''s degree in a life science discipline with a minimum of 2 years of relevant industry experience OR Bachelor''s degree in a life science discipline with a minimum of 4 years of relevant industry experience.
  • Experience using and developing cell-based assays with readouts such as ELISA, PCR or flow cytometry.
  • Excellent verbal and written communication skills.

Advantage if you possess:

  • Hands-on experience with development and validation of ELISA, PCR based-Bioassays and flow cytometry methods in a GxP setting.
  • Familiar with QbD principles and Design of Experiment approaches for method development/optimization.
  • A minimum of one year''s experience in a cGMP environment.

If this sounds like you, send your resume/CV to g.lafebre@nonstopconsulting.com

NonStop is one of the largest and fastest-growing specialized life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labor leasing licenses across Europe. Please visit our website for a full list of the niche markets we cover



Posted: 24/01/2022 | NPJ Ref: 296176
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