GxP - QC Lab Analyst

JR United Kingdom; England; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a QC Lab Analyst to ensure the highest quality standards are maintained. This role involves performing analysis, evaluation, and release of raw materials and finished goods while ensuring compliance with specifications. The ideal candidate will have a scientific background, experience in a QC setting, and strong problem-solving skills. Join a dynamic team where your contributions will directly impact product quality and safety, and be part of a collaborative environment that values continuous improvement and innovation.

Qualifications

• Bachelor's degree in a scientific field or equivalent experience required.
• Experience in QC or laboratory settings preferred.

Responsibilities

• Perform routine analysis of raw materials and finished goods.
• Conduct investigations for out of specification results.

Skills

Laboratory Testing

Attention to Detail

Problem-Solving

Communication Skills

Education

Bachelor's degree in a related scientific field

Tools

SAP

LIMS

Job description

The QC Lab Analyst is responsible for performing basic analysis, evaluation, and release of raw materials, mass, and/or cosmetic finished goods in compliance with specifications and standards. This includes conducting environmental monitoring testing, validating results, and performing investigations for Out of Specification (OOS) results. The role also involves providing feedback for improvements, updating SOPs, and training staff on new technical procedures. The QC Lab Analyst ensures the highest quality standards are maintained before materials are shipped or used in manufacturing.

Key Responsibilities:

Job Title: QC Lab Analyst

Location: Hmapshire

Department: Quality Control

Reports To: QC Lab Manager

Position Summary:

The QC Lab Analyst is responsible for performing analysis, evaluation, and release of raw materials, mass, and cosmetic finished goods in compliance with standards. This includes environmental monitoring, validating results, and investigating OOS results. The role also involves providing feedback, updating SOPs, and staff training to ensure quality before materials are shipped or used in manufacturing.

Key Responsibilities:

• Execution of QC Lab Testing (75%)

• Monitor Critical Control Parameters such as lab process water, pH, and balance through daily equipment verification checks.
• Perform routine and non-routine analysis of raw materials, mass, and finished goods, including sample preparation, testing, analysis, and reporting. This includes entering results into SAP/LIMS and preparing Certificates of Analysis (CoA).
• Conduct environmental monitoring testing and validation in compliance with regulatory standards.
• Ensure complete and accurate documentation for testing procedures and results.
• Collaborate with the Lab Coordinator to retain or discard samples, and ensure proper archiving of lab documents.

• Testing Data Review and Release (Varies by site)

• Review supporting test data and results, including sample preparation records, logbooks, calculations, and data sheets.
• Enter test results into SAP/LIMS and release raw materials, non-OTC mass, and cosmetic finished goods.

• Investigation and Problem Solving (15%)

• Identify quality-related issues and propose process improvements.
• Conduct Phase 1 OOS investigations under senior analyst guidance.
• Evaluate consumer complaints and Quality Inquiries to support QC decisions and corrective actions.

• SOP Development and Training (10%)

• Develop and update SOPs for QC testing processes.
• Provide training on new technical procedures to lab staff to ensure continuous improvement and adherence to quality standards.

Key Skills & Qualifications:

• Bachelor's degree in a related scientific field or equivalent experience.
• Experience in a QC or laboratory setting, preferably in pharmaceutical, cosmetic, or manufacturing industries.
• Familiarity with laboratory testing, sample preparation, and data entry systems (SAP/LIMS).
• Strong attention to detail and ability to follow strict protocols.
• Problem-solving skills and ability to suggest improvements.
• Good communication skills and team collaboration.
• Ability to work independently and manage priorities.

Additional Information:

• Participation in investigations and troubleshooting OOS results may be required.
• Training on new procedures will be provided as needed.
• Regular interaction with manufacturing and management departments is expected.