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Associate Device Testing Scientist

Cambridgeshire   •  Negotiable  •  Contract/Temporary, Full time


Associate Scientist Device Testing

6 month contract

Cambridge

19.29 per hour

Are you an experienced Scientist who has previously worked within Device testing? Cpl are working with one of the top pharma companies in the world who are currently recruiting for an experienced Scientist who can join their Device Development Sciences Team.

The Associate Scientist will provide support with tests and analysis of drug delivery devices, components and primary containers including syringes and cartridges.

Key responsibilities;

Hands-on testing of devices to generate data on the selected parameters, in accordance with the agreed protocols and methods, the testing will often involve the use of specialist techniques related to the specific drug delivery device
Responsible for a wide variety of laboratory tasks including developing test methods, experimental plans and trouble-shooting as needed
Operating laboratory equipment according to SOPs, Manuals, Methods and Risk assessments etc
Responsible for a wide variety of ISO 13485 related laboratory tasks including change control, instrument managing instrument compliance, inventory control and trouble-shooting as needed
Responsible for wide variety of tasks including aseptic techniques within filling of primary container closures and clinical setting
Maintains accurate records of results, analysis, and interpretation of experimental data in laboratory notebooks in a timely manner and according to accepted good practices
Uses tools to analyse, interpret and record data in order to quantify the functional performance characteristics of a device and controlling parameters for its consistent performance

Experience/ Qualifications;

Previous experience of working within a laboratory
Educated to a degree level within a Scientific or Engineering subject
Experience of working in teams in the development or trouble shooting of drug delivery devices, analytical methodology or manufacturing processes by means of designed experiments and logical problem solving
Experience of mechanical engineering equipment and methodology
Experience of GLP/GMP or ISO 13485

For more information please contact amy.goddard@cpl.com

  • Agency: Cpl Life Sciences
  • Reference: JO-2207-496828
  • Posted: 18th July 2022
  • Expires: 15th August 2022

Cpl Life Sciences

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