QC Chemist

Smart4Sciences; Ringway; On-site; GBP 32,000 - 42,000; Full time

Job summary

Science Solutions Recruitment Ltd is seeking a QC Chemist to join a GMP/ISO-regulated laboratory in Manchester. This role focuses on qualitative and quantitative analysis of materials, routine testing, and support for QA, production, and development activities.

You will contribute to method development, data interpretation and continuous improvement in a collaborative, fast-paced environment that emphasises quality and regulatory compliance.

Qualifications

• Experience in a Quality Control laboratory operating under GMP/ISO standards.
• Background in Analytical Chemistry or related discipline.
• Practical experience with at least one of: HPLC, GC, NMR, LC-MS, ICP-OES.

Responsibilities

• Conduct qualitative and quantitative chemical analysis of raw materials, intermediates and finished products.
• Perform sampling, sample preparation and analytical testing to support QC, Production and R&D.
• Carry out routine laboratory testing in line with GMP, ISO standards, SOPs and client requirements.
• Support analytical method development and continuous improvement initiatives.
• Maintain accurate, audit-ready laboratory records and documentation.
• Interpret, evaluate and communicate analytical results to internal teams, management and clients.
• Manage multiple testing priorities and deadlines while maintaining high analytical standards.
• Support the QC Manager and QC Team Leader with day-to-day laboratory operations.
• Promote Health & Safety, Quality and 5S standards within the laboratory.

Skills

GMP/ISO compliance

Analytical chemistry

Attention to detail

Independent and collaborative work

Time management

Education

Bachelor's degree in Analytical Chemistry

Tools

HPLC

GC

NMR

LC-MS

ICP-OES

Job description

QC Chemist

Location: Manchester, UK

Department: Quality Control & Analytics

Working Hours: Full-time

Salary: Competitive, dependent on experience

Are you an experienced Analytical Chemist with experience working within a GMP or ISO-regulated laboratory?

We are working with a pharmaceutical development and manufacturing organisation seeking a proactive and detail-oriented QC Chemist to join its Quality Control & Analytics team in Manchester.

This is an excellent opportunity to join a dynamic and collaborative environment, supporting manufacturing, research and development, and a diverse range of customer projects. You will play an important role in ensuring products meet the highest quality standards while contributing to scientific innovation and continuous improvement.

Key Responsibilities

• Conduct qualitative and quantitative chemical analysis of raw materials, intermediates and finished products.
• Perform material sampling, sample preparation and analytical testing to support QC, Production and PR&D activities.
• Carry out routine laboratory testing in accordance with GMP, ISO standards, SOPs and client requirements.
• Support analytical method development and continuous improvement initiatives.
• Maintain accurate, detailed and audit-ready laboratory records and project documentation.
• Interpret, evaluate and communicate analytical results to internal teams, management and clients where required.
• Manage multiple testing priorities and deadlines while maintaining accuracy and high analytical standards.
• Support the QC Manager and QC Team Leader with day-to-day laboratory operations.
• Promote and maintain Health & Safety, Quality and 5S standards within the laboratory.

Requirements & Experience

• Experience within a Quality Control laboratory operating under GMP and/or ISO-regulated standards.
• A background in Analytical Chemistry or a related scientific discipline.
• Practical experience with at least 1-2 of the following analytical techniques:
• HPLC (preferred)
• GC (preferred)
• NMR (preferred)
• LC-MS
• ICP-OES
• Strong practical laboratory and analytical chemistry skills.
• Excellent attention to detail and the ability to produce accurate and reliable analytical results.
• Strong organisational and time-management skills, with the ability to manage competing priorities.
• Confident written and verbal communication skills.
• Ability to work independently, including occasional lone working, as well as collaboratively within a team.
• A proactive approach to troubleshooting, problem-solving and continuous improvement.

Why Consider This Opportunity?

• Exposure to a varied range of analytical projects and customer requirements.
• Opportunity to develop your technical expertise within a collaborative laboratory environment.
• Involvement in manufacturing, research and development, and continuous improvement activities.

Interested?

If you have a background in Analytical Chemistry and experience working within a GMP or ISO-regulated QC laboratory, we would love to hear from you.