QC Analyst - Bioassay (12-Month Contract)
Pay Rate: £22.77 p/hr
Shift: 5 on 3 off
Location: Liverpool
Are you an analytical scientist with experience in GMP environments looking to develop your career within a fast-paced pharmaceutical setting? Do you thrive in high-throughput laboratories where precision, compliance, and attention to detail are critical? If so, this could be the ideal opportunity for you.
A leading pharmaceutical manufacturer is seeking a QC Analyst to join its Bioassay department. Supporting vaccine production on site, this role plays a key part in ensuring materials and products meet strict regulatory and quality standards.
Key Responsibilities:
Collecting samples from manufacturing areas and logging them into the laboratory system.
Performing laboratory testing, data review and data interpretation in accordance with approved SOPs.
Accurately recording and reporting analytical data in compliance with GMP and data integrity standards.
Carrying out routine maintenance and calibration of laboratory instrumentation.
Promptly escalating any issues, deviations, or atypical results (OOS/OOT/OOE) to senior staff.
Supporting and conducting laboratory investigations in collaboration with cross-functional teams.
Reviewing and updating SOPs as part of continuous compliance activities.
Completing HSE risk assessments and ensuring adherence to safety procedures.
Managing laboratory documentation, including archiving and record keeping.
What You’ll Need:
BSc in relevant scientific discipline.
At least 1 year of experience in an analytical laboratory, ideally within the pharmaceutical industry.
Strong understanding of cGMP and GDocP requirements.
Excellent attention to detail and ability to work accurately in a high-throughput environment.
Experience using LIMS/GLIMS systems (desirable).
What’s on Offer:
Competitive salary and benefits package
Opportunity to work within a highly regulated pharmaceutical environment
Ongoing training and development
On-site parking.
Subsidized canteen