QC Bioassay Analyst

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 Compliantly perform QC laboratory testing, data review and data interpretation in accordance with approved SOPs.

Analysis of in-process, intermediate and finished vaccine products. Participate in technical and validation studies supporting departmental and site objectives. Comply with cGMP and GDocP regulations to maintain compliance.

Perform primary QC inspection, sampling of raw materials and components, and laboratory testing. Support release of raw materials and components for use in manufacture. Perform analytical testing of raw materials, in-process, finished product and utilities samples in accordance with relevant SOPs.

Conduct instrument maintenance and calibration. Escalate any OOS/OOE/OOT results to Team Coordinator/Laboratory Manager as soon as practically possible. Initiate and perform laboratory investigations in collaboration with relevant departments.

Qualifications BSc in an equivalent scientific discipline, ideally chemistry. Recent experience in a cGMP pharmaceutical lab performing analytical QC bioassay testing for at least 1 year. #J-18808-Ljbffr