An exciting opportunity has risen for a QC Analyst to join a global pharmaceutical company within their bioassay lab, within QC.
Job Title: QC Bioassay Analyst
Vacancy type: Temporary role expected to last around 6 months (5 on 3 off shift pattern)
Area: Liverpool
Salary: Highly competitive
SRG is working with a leading global pharmaceutical company who require a QC Bioassay Analyst to join their well-established QC lab. 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). 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:
The purpose of the QC Incoming and Components Analyst role is to compliantly perform Primary QC inspection, Sampling of raw materials, components laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs) for all primary and secondary packaging components.
QC Incoming and components analysts will be required to support release of raw materials and components for use in manufacture. QC incoming and component's Analysts may also be required to participate in technical and validation studies in support of both departmental and site objectives.
Work to a high level of cGMP and GDocP in order to maintain compliance and adherence to regulations.
Perform analytical testing of raw materials, in process, finished product and utilities samples in accordance with relevant SOPs.
Instrument Maintenance and Calibration
Escalate any OOS/OOE/OOT results to Team Co-Ordinator/Laboratory Manager as soon as practically possible.
Initiate and perform laboratory investigations with discussion and collaboration with effected departments where necessary.
Applicant requirements:
BSc in equivalent in Scientific discipline, ideally chemistry.
Recent experience in a cGMP pharmaceutical lab performing analytical QC bioassay testing for at least 1 year.
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