Associate QC Analyst

hays-gcj-v4-pd-online; England; On-site; GBP 25,000 - 35,000; Full time

Job summary

Join a global diagnostics organization as an Associate QC Analyst, ensuring quality control of raw materials and finished products. This hands-on role is ideal for those with a passion for quality, offering a supportive environment with growth opportunities and a strong commitment to innovation.

Benefits

Generous paid time off and public holidays

Competitive salary and comprehensive benefits package

Opportunities for growth and development

Supportive team environment committed to quality

Qualifications

• Minimum 2 years of experience in a QC or laboratory environment.
• Strong analytical and problem-solving skills.

Responsibilities

• Perform analytical testing and maintain documentation.
• Support laboratory investigations and manage OOS results.

Skills

Analytical

Problem Solving

Attention to Detail

Communication

Job description

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Your Newpany
You will be joining a global diagnostics organisation committed to improving patient outcomes through innovation and quality. Based in Maidstone, Kent, the company offers a collaborative, mission-driven culture and a unique opportunity to contribute to the future of healthcare diagnostics.

Your New Role

As an Associate QC Analyst, you will play a key role in ensuring the quality and compliance of raw materials, in-process materials, and finished products. You will perform scientific analyses, support laboratory investigations, and contribute to continuous improvement initiatives. This is a hands-on role ideal for someone with a meticulous approach and a passion for quality in a regulated environment.

Main Responsibilities

• Quality Control Testing: Perform analytical testing on raw materials, intermediates, and final products to ensure compliance with established specifications.
• Documentation: Maintain accurate and detailed records of laboratory work in accordance with company procedures and regulatory standards.
• Investigation Support: Apply technical knowledge to support laboratory investigations and troubleshoot issues as they arise.
• Out of Specification (OOS) and Non-Conformance (NC) Management: Participate in managing OOS results, NCs, Change Controls, and CAPAs.
• SOP Management: Assist in reviewing and developing Standard Operating Procedures (SOPs) and ensure adherence to quality standards.
• Project Involvement: Lead or support QC projects such as method improvements, Kaizen initiatives, and Six Sigma activities.
• Equipment Maintenance: Ensure laboratory instruments and equipment are calibrated, maintained, and in good working order.
• Product Release: Review completed product workbooks to support timely product release.

What You’ll Need to Succeed

• Experience: Minimum 2 years of relevant experience in a QC or laboratory environment, with exposure to regulated industry practices.
• Technical Skills: Strong analytical and problem-solving skills, with the ability to interpret data and troubleshoot effectively.
• Attention to Detail: Diligent and methodical approach to laboratory work and documentation.
• Communication: Confident and credible communicator, able to work collaboratively across teams.
• Desirable: Experience with proficiency surveys, certification programs, and continuous improvement methodologies.

What You’ll Get in Return

• Holidays: Generous paid time off and public holidays.
• Benefits: Competitive salary and comprehensive benefits package.
• Opportunities: Be part of a global diagnostics leader with opportunities for growth and development.
• Environment: Supportive, quality-focused team environment with a strong commitment to innovation and excellence.

What You Need to Do Now

If you are passionate about quality and ready to contribute to a dynamic and innovative team, please click ‘apply now’ or contact us on [phone] for a confidential discussion. If this role isn’t quite right for you, we’d still love to hear from you to explore other opportunities.

Keywords: Quality Control, QC Analyst, Laboratory Testing, Diagnostics, GMP, SOP, Product Release, Continuous Improvement, CAPA, Kaizen, Six Sigma

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