£ 16.48 - £ 17 / Hourly
Science - Microbiology
· Job type
· External Reference
Please note this role is working a 4 on 4 off shift. 11 Hour days. 12 Month Contract
To operate within the required standards of HSE (Awareness of Risk Assessments, Accidents, Incidents, Near Misses, NOSIs) and company Quality Systems and policies in accordance with CFR regulations.
Perform accurate and reliable laboratory tests and generate results to cGMP standard by entering and authorising test data. Including the investigation of any invalid, OOS/OOT results within the GLIMS system, in accordance with current company requirements and SOPs. To consult with QA and where required initiate Sentry investigations where deviations have occurred. To ensure that the maintenance, qualification and calibration of laboratory equipment used is up to date and at the required GMP standards. To use only approved and validated assay processes and reagents.
Participate in laboratory administration, including the complete and review of log books and PCS alarms generated progression of Change Controls, SOP reviews and closure of assigned Corrective/Preventative actions. To participate in department housekeeping activities, such as cleaning, ordering and maintenance of stocks.
To participate in planning and execution of ad hoc projects such as technical and validation studies. To troubleshoot in the resolution of testing problems where required.
Fluent in English
Experienced in the relevant testing discipline within the Pharmaceutical industry
Experience of Quality Control testing techniques.
Experience in cGMP environment or Industry practices
Awareness of test and equipment validation
Knowledge of continuous improvement and root cause analysis techniques
Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.
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Please apply with your CV to: andrea redmond