QC Analyst

Orion Group Life Sciences are currently recruiting a QC Analyst on behalf of our Multinational Pharmaceutical client based in Liverpool on an initial 6-month contract with strong potential to extend.
 
Role Overview
The QC Analyst is responsible for performing laboratory testing, data review, and interpretation in compliance with cGMP standards and approved SOPs. Testing will include in-process, intermediate, and finished products, as well as raw materials and packaging components.
 
Key Responsibilities
Laboratory Testing & Compliance

• Perform analytical testing, data review, and interpretation in line with approved SOPs and cGMP standards.
• Ensure all work complies with regulatory requirements (EU GMP, FDA) and health & safety standards.
• Accurately document and report results in a timely manner.
• Promptly escalate deviations, out-of-specification (OOS) results, or compliance issues to the QC leadership team.

 
Quality Systems & Technical Support

• Perform instrument calibration and maintenance.
• Support reagent and standard qualification.
• Raise and support deviations, CAPAs, and change controls.
• Review and update SOPs and documentation.
• Participate in risk assessments and validation activities.

 
Laboratory Operations & Administration

• Maintain laboratory documentation and archives.
• Manage inventory, reagents, and consumables.
• Support sample management and storage activities.
• Ensure a clean, safe, and compliant working environment.

 
Additional Responsibilities

• Maintain up-to-date training records and only perform tasks within training scope.
• Communicate effectively with team members and cross-functional stakeholders.
• Participate in continuous improvement initiatives and support team objectives.
• Undertake additional duties as required.

 
Scope & Accountability

• No direct reports.
• Responsible for accuracy, compliance, and quality of own work.
• Accountable for identifying and escalating non-compliance or deviations.
• Contributes to cost awareness and operational efficiency.

 
Key Relationships

• QC teams (Bioassay, Analytical, Microbiology, Stability, Sample Management)
• Quality Assurance (QA)
• Manufacturing and Engineering
• Supply Chain and Planning

 
Decision Making & Problem Solving

• Identify and escalate issues relating to:
  • Testing or equipment failures
  • Out-of-specification or invalid results
  • Compliance gaps
• Apply a risk-based approach to prioritisation and resolution.
• Support investigations and contribute to root cause analysis.

Skills & Experience
Essential

• Experience working in a GMP-regulated laboratory environment
• Knowledge of QC testing techniques relevant to the role
• Understanding of data integrity and documentation standards
• Familiarity with equipment and method validation principles
• Strong attention to detail and problem-solving skills
• Good communication and teamwork abilities
• Computer literate with experience using electronic systems

 
Education & Experience

• Degree or equivalent qualification in a relevant scientific discipline
• Prior experience in a QC or laboratory-based role, ideally within the pharmaceutical or related industry

 


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Orion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.