Quality Control Analyst - Bioassay

Job Title: QC Bioassay Analyst Vacancy type: Temporary role expected to last around 6 months (5 on 3 off) Area: Liverpool Salary: Highly competitive An exciting opportunity has arisen for a QC Analyst to join a global pharmaceutical company within their bioassay lab, within QC. SRG is working with a leading global pharmaceutical company that requires 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 Primary QC inspection, sampling of raw materials, components laboratory testing, data review and data interpretation in accordance with approved SOPs for all primary and secondary packaging components.

Support release of raw materials and components for use in manufacture. Participate in technical and validation studies in support of both departmental and site objectives. Work to a high level of cGMP and GDocP 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 practicably possible.

Initiate and perform laboratory investigations with discussion and collaboration with affected departments where necessary. Qualifications BSc in an equivalent scientific discipline, ideally chemistry. Recent experience in a cGMP pharmaceutical laboratory performing analytical QC bioassay testing for at least 1 year. #J-18808-Ljbffr