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QC Bioassay Analyst

Job Posted: 7 days ago

Salary: £ 22.77 - 22.77 / Hour
Job Type: Contract
Location: North West

Expire in: 21 days

Job Description

QC Bioassay / Incoming & Components Analyst
📍 Location: Merseyside
📅 Contract: 6 Months
🏢 Company: Global Biopharmaceutical Organisation
Overview
We are supporting a global biopharmaceutical organisation based in Liverpool in the search for an experienced QC Analyst to join their Quality Control team on a 6-month contract.
This role will focus on the compliant execution of QC testing, inspection, and release activities across both bioassay and incoming materials/components, supporting critical vaccine manufacturing operations.
You will also contribute to technical and validation studies, ensuring alignment with both departmental and site objectives.
Key Responsibilities
QC Bioassay
  * Perform QC testing on in-process, intermediate, and finished vaccine products
  * Conduct data review and interpretation in line with approved SOPs
  * Ensure all work is carried out in compliance with cGMP and regulatory standards
  * Accurately document all laboratory activities, ensuring data integrity
  * Support method validation, transfer, and technical studies
QC Incoming & Components
  * Perform primary QC inspection and sampling of raw materials
  * Conduct testing of primary and secondary packaging components
  * Review and interpret analytical data in accordance with SOPs
  * Support the release of raw materials and components for manufacturing
  * Assist in deviations, investigations, and CAPA activities
Requirements
  * Fluent in English (written and verbal)
  * Proven experience in QC testing techniques relevant to the role (bioassay and/or raw materials/components testing)
  * Strong experience working within a cGMP-regulated environment
  * Clear understanding of GMP compliance, documentation, and data integrity principles
  * Awareness of equipment qualification and method validation requirements
  * Understanding of root cause analysis and its application within investigations
  * Strong IT skills with experience using electronic laboratory and quality systems (e.g. LIMS, electronic documentation systems)
  * Demonstrable experience working within the pharmaceutical or biopharmaceutical industry under cGMP conditions

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