Senior QC Analyst

Nexus Life Sciences

Ringway

On-site

GBP 30,000 - 35,000

Full time

3 days ago
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Benefits offered by this job

Competitive pay for the duration of 6‑
Dynamic pharma environment
Leadership role in QC
Impactful pharmaceutical products

Job summary

Nexus Life Sciences is seeking a Senior QC Analyst for a 6-month fixed-term contract in the United Kingdom. The role focuses on leading QC laboratory activities, ensuring GMP/GLP compliance, and releasing products through analytical testing using HPLC and GC.

The ideal candidate has a degree in Chemical Sciences and at least 5 years of GMP QC/Analytical experience, with strong communication and problem-solving abilities. Proactive leadership and adherence to safety protocols are essential.

Qualifications

  • Degree in Chemical Sciences or equivalent practical experience.
  • Minimum 5 years of Quality Control/Analytical experience within a GMP environment.
  • Proficiency with HPLC/GC and spectroscopy techniques.
  • Strong analytical thinking and problem-solving skills.

Responsibilities

  • Supervising and leading a team of analysts in the QC laboratory, ensuring GMP/GLP compliance.
  • Reviewing Batch Manufacturing Documents and analytical results for product release.
  • Performing analytical testing of samples for release, stability, and validation with HPLC/GC.
  • Assigning duties to analysts based on release requirements and maintaining lab operations.
  • Reviewing and approving product labels for Production use.
  • Preparing and reviewing SOPs, Raw Material Documents, Analytical Test Reports, and Validation Protocols.
  • Providing technical support and troubleshooting analytical methods; maintaining equipment.
  • Ensuring laboratory housekeeping meets required standards.
  • Supporting inspection readiness and promoting continuous improvement.
  • Collaborating with QA and Production teams for seamless operations.
  • Reviewing analytical data against pharmacopeial specifications.

Skills

Analytical thinking
Troubleshooting
Attention to detail
Excellent communication

Education

Degree in Chemical Sciences

Tools

HPLC
GC
IR spectroscopy
NIR spectroscopy

Job description

Job Advertisement: Senior QC Analyst (6-Month FTC Contract Role)
Overview

Salary £30,000 - £35,000 pro rata

We are seeking a highly skilled and experienced Senior QC Analyst for a 6-month fixed-term contract to join a pharmaceutical manufacturing organisation.

Reporting directly to the QC Manager, this role is integral to ensuring the quality and compliance of pharmaceutical products.

Responsibilities
  • Supervising and leading a team of analysts in the Quality Control laboratory, ensuring compliance with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).
  • Reviewing Batch Manufacturing Documents and analytical test results to facilitate product release.
  • Performing analytical testing of manufactured product samples for release, stability studies, and validation using techniques such as HPLC and GC.
  • Assigning duties to analysts based on production release requirements, ensuring efficient laboratory operations.
  • Reviewing and approving product labels for use by the Production Department.
  • Preparing and reviewing Standard Operating Procedures, Raw Material Documents, Analytical Test Reports, Validation Protocols, and Reports.
  • Providing technical support, troubleshooting analytical methods, and maintaining laboratory equipment.
  • Ensuring laboratory housekeeping is maintained to appropriate standards.
  • Supporting inspection readiness and promoting a culture of continuous improvement.
  • Collaborating with Quality Assurance and Production teams to ensure seamless operations.
  • Reviewing analytical data against pharmacopeial and registered specifications.
Qualifications
  • A degree in Chemical Sciences or equivalent practical experience.
  • A minimum of 5 years of Quality Control/Analytical experience within a GMP environment.
  • Proficiency in analytical techniques, including IR and NIR spectroscopy, High-Performance Liquid Chromatography (HPLC), and Gas Chromatography (GC).
  • Strong analytical thinking, problem-solving, and troubleshooting skills.
  • Excellent communication skills, both verbal and written, with a keen eye for detail.
  • Good computer literacy and familiarity with laboratory systems.
  • A commitment to health and safety practices, including ensuring team members are adequately trained in safety protocols and the use of PPE.
Benefits
  • Competitive compensation for the duration of the 6-month fixed-term contract.
  • Opportunity to work in a dynamic and well-established pharmaceutical manufacturing environment.
  • Gain valuable experience in a leadership role within a Quality Control function.
  • Contribute to the production of high-quality pharmaceutical products that make a difference in people's lives.

Note: No sponsorship is available for this position

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