QC Radiochemist - 12 month FTC

QC Chemist | Woking, Surrey | Permanent

Join a dynamic team as a QC Chemist/ Analyst at an esteemed international pharmaceutical company in this new permanent role.

In this role, you'll gain training in a niche area of chemistry, contributing to a rapidly growing field. You'll have the opportunity to develop your skills and advance in your career while enjoying competitive remuneration. The ideal candidate will have worked in a pharmaceutical GMP laboratory previously – ideally with chromatography equipment.

This position involves shift work, so flexibility is key. The shift pattern rotates weekly as follows: 3am, 6am, 6am, 8am, 8am.

Key requirements:

• A degree in a Life Sciences discipline or equivalent

• Previous QC chemistry work experience in industry

• Familiarity with chromatography techniques such as HPLC and GC

• Understanding of GMP principles is preferred

• Flexibility to work shifts

If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below for more information.

Keywords: QC, quality control, analyst, analytical, laboratory, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work.

🔬 QC Analyst | South London | Pharmaceutical Manufacturing

Looking for your next opportunity in Quality Control?

We're partnering with a pharmaceutical manufacturer seeking a QC Analyst to join a busy and growing Quality team. This is a fantastic opportunity for someone with analytical laboratory experience who enjoys working in a GMP-regulated environment and wants to contribute to product quality, compliance, and continuous improvement.

What you'll be doing:

✅ Testing raw materials, packaging components, in-process samples, and finished products
✅ Performing analytical testing using HPLC and GC techniques
✅ Supporting laboratory validation, calibration, and maintenance activities
✅ Conducting environmental monitoring and water sampling
✅ Investigating OOS results and supporting quality investigations
✅ Maintaining GMP-compliant documentation and data integrity standards
✅ Performing in-process quality inspections and production line checks
✅ Working closely with Quality, Production, and other cross-functional teams

What we're looking for:

✔ Degree in a Scientific discipline or equivalent
✔ Experience working within an analytical laboratory environment
✔ Strong understanding of GMP and Data Integrity requirements
✔ Hands-on experience with HPLC and GC, including troubleshooting instrumentation
✔ Excellent documentation and report-writing skills
✔ Strong attention to detail and a proactive approach to quality

This role would suit candidates from pharmaceutical, biotech, medical device, FMCG, food, or other regulated manufacturing environments who are looking to further develop their career within Quality Control.

📩 Interested in finding out more? Apply now or get in touch for a confidential discussion.

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QC Supervisor

Join a thriving team as a QC Supervisor at an esteemed international pharmaceutical company in this newly created permanent role.

This is an excellent opportunity for an experienced QC professional looking to take the next step into leadership. You'll be responsible for supervising a team of QC Chemists and Analysts, providing coaching and technical guidance, coordinating laboratory activities, and deputising for the QC Manager when required.

Working within a GMP-regulated laboratory, you'll play a key role in ensuring testing is completed to high quality standards while supporting the ongoing development of the team. The ideal candidate will have previous pharmaceutical QC experience and strong knowledge of analytical techniques such as HPLC and GC.

This position involves working 8 hour days from 6am or 8am – with flexibility required for the applicant to be available to work either shift,

Key Responsibilities

• Supervise and coordinate the daily activities of the QC laboratory team.

• Coach, mentor, and develop QC Chemists.

• Ensure testing is performed in compliance with GMP requirements and laboratory procedures.

• Support laboratory investigations, deviations, and OOS activities.

• Review data and documentation to ensure accuracy and compliance.

• Assist with workload planning and resource allocation.

• Deputise for the QC Manager when required.

• Drive continuous improvement initiatives within the laboratory.

Key Requirements

• Degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related discipline.

• Circa 5 years+ experience working within a pharmaceutical GMP QC laboratory.

• Hands-on experience with analytical techniques such as HPLC and GC.

• Previous supervisory, mentoring, or team leadership is an advantage.

• Strong understanding of GMP and quality compliance requirements.

• Excellent communication and organisational skills.

If you're looking to progress your leadership career within a growing pharmaceutical business while remaining hands-on in a laboratory environment, apply below for more information.

Keywords: QC Supervisor, Quality Control Supervisor, Laboratory Supervisor, QC Team Leader, Analytical Chemist, HPLC, GC, GMP, Pharmaceutical, Biotechnology, Laboratory Management, Quality Control, Team Leadership, Pharmaceutical Manufacturing.

QC Chemist

Join a dynamic team as a QC Chemist/ Analyst at an esteemed international pharmaceutical company in this new permanent role.

In this role, you'll gain training in a niche area of chemistry, contributing to a rapidly growing field. You'll have the opportunity to develop your skills and advance in your career while enjoying competitive remuneration. The ideal candidate will have worked in a pharmaceutical GMP laboratory previously – ideally with chromatography equipment.

This position involves shift work, so flexibility is key. The shift pattern rotates weekly as follows: 3am, 6am, 6am, 8am, 8am.

Key requirements:

• A degree in a Life Sciences discipline or equivalent

• Previous QC chemistry work experience in industry

• Familiarity with chromatography techniques such as HPLC and GC

• Understanding of GMP principles is preferred

• Flexibility to work shifts

If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below for more information.

Keywords: QC, quality control, analyst, analytical, laboratory, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work.

Engineering Manager

📍 Rotherham, South Yorkshire

Ready to take ownership of a site's engineering function and make a real impact?

We're partnering with a leading pharmaceutical manufacturer looking for an experienced Engineering Manager to drive reliability, performance, and continuous improvement across a critical production facility.

This role would suit an engineering leader from a pharmaceutical, biotech, FMCG, or regulated manufacturing environment who enjoys managing high-performing teams, improving asset reliability, and leading engineering strategy.

What you'll be doing:

🔹 Leading maintenance, facilities, utilities, and asset management activities
🔹 Driving equipment reliability and preventative maintenance programmes
🔹 Managing CAPEX projects, upgrades, and site improvement initiatives
🔹 Leading fault investigations, root cause analysis, and corrective actions
🔹 Developing and mentoring engineering teams
🔹 Ensuring engineering compliance and operational excellence

What we're looking for:

✅ Engineering leadership experience within pharma, biotech, FMCG, or manufacturing
✅ Strong maintenance, reliability, and asset management background
✅ Experience managing production equipment, facilities, and utilities
✅ A proactive leader with a continuous improvement mindset

If you're looking for a role where you can influence site strategy, lead impactful projects, and help shape the future of a growing operation, I'd be delighted to speak with you.

📩 Apply now or send me a direct message for a confidential discussion.

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Quality Supervisor

📍 Trefriw, North Wales | Permanent | On-site

🏭 GMP Healthcare Manufacturing

An exciting opportunity for an experienced Quality professional to oversee QA and QC activities within a growing GMP manufacturing facility. Reporting into site leadership, you'll supervise a small quality team, ensure GMP compliance, lead investigations, and drive continuous improvement across the site.

Key Responsibilities

• Supervise QA & QC operations and manage a team of 2

• Ensure GMP compliance and quality system effectiveness

• Lead deviations, CAPAs, non-conformances and complaint investigations

• Review batch records, SOPs and quality documentation

• Support audits, inspections, change controls and validations

• Monitor KPIs and promote a strong quality culture

• Collaborate with Manufacturing and Operations teams

Requirements

• GMP manufacturing experience

• Previous supervisory or team leadership experience

• Strong QA/QC knowledge

• Experience with deviations, CAPAs and non-conformances

• Excellent communication and organisational skills

What’s on Offer

• Broad QA/QC leadership role

• Supportive and growing business

• Long-term career development opportunities

• Competitive salary and benefits package