Overview

Reference Number: JO-2311-526279
QC Analyst Bioassay
Rate: Negotiable
Job Type: Contract
Location: Liverpool

QC Analyst Bioassay

12 Month Contract, not required for the month of February

£19.99 per hour

Liverpool, Speke

44hr, 5on / 3off shift ( 08:00 – 17:00 on day 1 to 4, 08:00 – 16:00 on day 5)

Cpl Life Sciences are currently recruiting for a global pharmaceutical company that focusses on the development and manufacturing of life changing vaccines recruiting for a QC Analyst to join their Quality (Bioassay) laboratory.

 

The purpose of the QC Bioassay analyst role is to compliantly perform QC laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs) to support with product release. Analysis is performed on in-process, intermediate and finished vaccine products. QC Bioassay analysts are also required to participate in technical and validation studies in support of both departmental and site objectives.

Responsibilities;

• Instrument Maintenance and Calibration

• Reagent and Standard Qualification

• Initiation of deviations

• Initiation, and completion, of CAPAs

• Completion of Change Control actions

• Updates and reviews of SOPs

• Participation in quality risk assessments

• HSE risk assessment completion, review and adherence

• Archiving of laboratory documentation,

• Ordering of reagents and consumables

• Maintenance of QC sample and reagent stores

• Ensuring a clean and safe workplace for all associates

Requirements/ Experience;

• Have experience in QC testing techniques, preferably Bioassay experience

• Have experience in cGMP application

• Have an awareness of the requirements for equipment and method validation

 

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

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here