QC Analyst

QC Analyst (12-Month Contract)Pay Rate: £22.77 p/hrShift: 4 on 4 offLocation: 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 Analytical and Raw Materials Laboratory. 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 analytical testing of raw materials, in-process samples, finished products, and utilities in line with approved methods and procedures.
• 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 Chemistry or related subject (or equivalent).
• 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.

What’s on Offer:

• Competitive salary and benefits package.
• Opportunity to work within a highly regulated pharmaceutical environment.

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