QC Materials Analyst

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

Job summary

An established industry player is seeking a QC Materials Analyst to join their dynamic team in London. This role offers the chance to manage incoming materials and ensure they meet stringent quality standards for manufacturing. You will play a vital role in supporting the Quality Control Materials Team, maintaining compliance with Good Manufacturing Practice (GMP), and enhancing operational efficiencies. If you are passionate about science and innovation and have a keen eye for detail, this opportunity could be your next career step in the biologics industry.

Qualifications

• Experience in a GMP environment is essential.
• Strong attention to detail and quality management skills required.

Responsibilities

• Check incoming materials for quality standards.
• Maintain accurate records and ensure compliance with GMP.
• Organize testing for new materials as needed.

Skills

GMP experience

Attention to detail

Problem-solving

Effective communication

Task organization

Microsoft Office proficiency

Tools

Microsoft Office

Job description

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Passionate about science and innovation? Your dream job awaits in the biologics industry!

Hobson Prior is seeking a QC Materials Analyst to join our client's team in London. In this role, you will manage incoming materials and ensure they meet quality standards for manufacturing. You will support the Quality Control Materials Team and help maintain compliance with Good Manufacturing Practice (GMP).

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Check incoming materials to ensure they meet quality standards.
• Keep track of material inspections and ensure they are suitable for production.
• Make sure storage conditions are appropriate for materials.
• Organize testing for new materials when needed.
• Maintain accurate records of all materials.
• Ensure materials are approved or rejected as needed.
• Follow health, safety, and GMP procedures.
• Report any issues or deviations from procedures.
• Help plan tasks to ensure timely delivery of products.
• Support improvements in methods and technology.

Key Skills and Requirements:

• Experience working in a GMP environment.
• Strong attention to detail and quality management skills.
• Problem-solving abilities and effective communication skills.
• Ability to organize and prioritize tasks efficiently.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint) is preferred.

For more information, please contact Danielle Hull.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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