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Senior QC Analyst
Added 05/11/2026
Reference: JN -112026-87865_1793877171

Are you a quality-driven scientist with a keen eye for detail and a passion for analytical chemistry?Smart4Sciences is... Read more

Are you a quality-driven scientist with a keen eye for detail and a passion for analytical chemistry?

Smart4Sciences is recruiting for a Senior QC Analyst to join one of the UK's leading generic pharmaceutical manufacturers. This is an excellent opportunity for a motivated scientist to develop their career within a GMP-regulated Quality Control environment, supporting the testing and release of products that make a real difference to patients' lives.

The Role

As a Senior QC Analyst, you will be responsible for supporting Quality Control activities through the validation, verification, and execution of analytical methods. Working within a collaborative laboratory team, you will help ensure the quality, safety, and compliance of raw materials, components, and finished pharmaceutical products.

Key responsibilities include:

Designing and executing analytical method validation and verification studiesPerforming routine analysis using techniques such as HPLC, UPLC, GC, and UVSupporting the monitoring of raw materials, components, in-process samples, and finished productsPreparing validation protocols, reports, and technical documentationEnsuring compliance with GMP, Health & Safety, and COSHH requirementsSupporting continuous improvement initiatives within the QC laboratoryAssisting with laboratory investigations and troubleshooting activities where requiredThe Candidate

We are keen to speak with candidates who possess:

A degree in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related scientific disciplineExperience within a pharmaceutical or regulated laboratory environmentDemonstrable experience in analytical method validation and/or verificationKnowledge of analytical techniques including HPLC, UPLC, GC, and UVA strong understanding of GMP, Health & Safety, and COSHH regulationsExcellent attention to detail and scientific problem-solving skillsThe ability to work independently and as part of a collaborative teamPrevious supervisory or mentoring experience would be advantageousWhy Apply?

This is a fantastic opportunity to join a well-established pharmaceutical organisation known for its commitment to quality and innovation. You'll gain exposure to a wide range of analytical techniques, work alongside experienced scientists, and play a key role in ensuring the delivery of safe and effective medicines. The role offers excellent opportunities for professional development and career progression within Quality Control and Analytical Sciences.

If you're looking to advance your career in pharmaceutical Quality Control and analytical chemistry, we'd love to hear from you.

Read less
£10,000.00 - £20,000.00
Per annum

Wrexham, Wales, United KingdomFull Time

QC Stability Lead (Senior QC Analyst )
Added 09/09/2026
Reference: JN -082026-87345_1788939745

About the RoleSmart4Sciences is working with a leading healthcare organisation to recruit a QC Stability Lead to join... Read more

About the Role

Smart4Sciences is working with a leading healthcare organisation to recruit a QC Stability Lead to join their Quality Control team in Hull.

This is an excellent opportunity for an experienced QC Analyst / Pharmaceutical Analyst looking to take on a lead-level position. You will join a team of 8 analysts, providing technical and troubleshooting support across laboratory equipment, analytical methods and systems.

Key Responsibilities
Provide technical support and troubleshooting guidance to the QC analytical team.Support troubleshooting of laboratory equipment, systems and analytical methods.Carry out pharmaceutical analysis in accordance with GMP requirements.Perform analytical testing using techniques including HPLC, GC and Karl Fischer.Provide technical guidance and support to other analysts within the team.Assist with analytical method troubleshooting where required.Ensure laboratory activities are carried out in accordance with GMP requirements and relevant procedures.Work closely with the Head of QC to support the effective technical operation of the laboratory.
About you:
Strong experience within pharmaceutical QC/analytical testing.Hands-on experience with HPLC, GC and Karl Fischer.Experience working within a GMP-accredited laboratory environment.Strong analytical troubleshooting and problem-solving skills.Experience troubleshooting laboratory equipment, systems and analytical methods.The confidence to provide technical guidance and support to other analysts.Excellent attention to detail and a methodical approach to laboratory work.Apply Now

If you are an experienced pharmaceutical analyst with strong analytical and troubleshooting experience and are looking for the next step in your QC career, we would be keen to hear from you.

Read less
£30,000.00 - £35,000.00
Per annum

Hull, England, United KingdomPermanent

QC Stability Lead (Senior QC Analyst )
Added 14/08/2026
Reference: JN -082026-87345_1786715920

About the RoleSmart4Sciences is working with a leading healthcare organisation to recruit a QC Stability Lead to join... Read more

About the Role

Smart4Sciences is working with a leading healthcare organisation to recruit a QC Stability Lead to join their Quality Control team in Hull.

This is an excellent opportunity for an experienced QC Analyst / Pharmaceutical Analyst looking to take on a lead-level position. You will join a team of 8 analysts, providing technical and troubleshooting support across laboratory equipment, analytical methods and systems.

Key Responsibilities
Provide technical support and troubleshooting guidance to the QC analytical team.Support troubleshooting of laboratory equipment, systems and analytical methods.Carry out pharmaceutical analysis in accordance with GMP requirements.Perform analytical testing using techniques including HPLC, GC and Karl Fischer.Provide technical guidance and support to other analysts within the team.Assist with analytical method troubleshooting where required.Ensure laboratory activities are carried out in accordance with GMP requirements and relevant procedures.Work closely with the Head of QC to support the effective technical operation of the laboratory.
About you:
Strong experience within pharmaceutical QC/analytical testing.Hands-on experience with HPLC, GC and Karl Fischer.Experience working within a GMP-accredited laboratory environment.Strong analytical troubleshooting and problem-solving skills.Experience troubleshooting laboratory equipment, systems and analytical methods.The confidence to provide technical guidance and support to other analysts.Excellent attention to detail and a methodical approach to laboratory work.Apply Now

If you are an experienced pharmaceutical analyst with strong analytical and troubleshooting experience and are looking for the next step in your QC career, we would be keen to hear from you.

Read less
£30,000.00 - £35,000.00
Per annum

Hull, England, United KingdomPermanent

Senior QC Analyst
Added 15/07/2026
Reference: JN -042026-86554_1784130267

Smart4 Sciences is partnering with a leading pharmaceutical manufacturer in St Albans to recruit a Senior QC Analyst... Read more

Smart4 Sciences is partnering with a leading pharmaceutical manufacturer in St Albans to recruit a Senior QC Analyst who will play a key role in supporting Quality Control operations and ensuring products are tested to the highest GMP and regulatory standards.

You'll be joining a collaborative QC team where you'll play a key role in ensuring raw materials, in-process samples and finished products meet the highest quality standards while supporting continuous improvement and regulatory compliance.

The Role

Your responsibilities will include:

Performing analytical testing on raw materials, in-process samples and finished productsOperating and troubleshooting HPLC, Karl Fischer Titration, Dissolution and other analytical equipmentCarrying out physical testing of tablets, capsules and packaging materialsPreparing, reviewing and checking analytical data prior to approvalPeer reviewing laboratory documentation and analytical resultsSupporting the review and update of SOPs, specifications and analytical proceduresEnsuring compliance with GMP, Data Integrity and Good Documentation PracticesMaintaining laboratory equipment, reference standards and consumablesSupporting investigations relating to analytical issues and implementing corrective actionsCompleting allocated training and maintaining competency across analytical techniques
What we are looking for :EssentialDegree, Diploma or Certificate in Chemistry, Analytical Science, Medical Laboratory Science or a related scientific disciplinePrevious experience working within a pharmaceutical QC laboratoryHands-on experience with HPLC analysisExperience using a range of laboratory instrumentation and analytical techniquesStrong understanding of GMP, Data Integrity and Good Documentation PracticesExcellent attention to detail and analytical skillsStrong written and verbal communication skillsDesirableExperience with Agilent HPLC systems and OpenLab softwareExperience with Karl Fischer Titration, Dissolution testing and physical testing of pharmaceutical dosage formsExperience reviewing analytical data and laboratory documentationPrevious experience supporting SOP reviews and method improvements

If you're an experienced QC Analyst looking for your next challenge in pharmaceutical manufacturing, we'd love to hear from you.

Read less
£32,000.00
Per annum

Hertfordshire, United KingdomPermanent

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