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 RoleYour 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 techniquesAre you a detail‑driven laboratory professional with a passion for maintaining high standards in a regulated scientific environment?Smart4... Read more
Are you a detail‑driven laboratory professional with a passion for maintaining high standards in a regulated scientific environment?
Smart4 Sciences are working with a well‑established and innovative specialist in pharmaceutical formulation and product development to recruit a Senior QC Analyst to join their quality control team.
The Role
This is a hands‑on opportunity to lead and support analytical activities within a GMP‑regulated laboratory environment. You will play a key role in ensuring the accurate sampling, testing, and reporting of raw materials, intermediates, and finished products, while maintaining compliance with GMP and ALCOA+ principles.
You will also provide supervision and mentorship to team members, supporting onboarding, training, and continuous improvement across laboratory operations.
Key Responsibilities
Lead and perform sampling, testing, and reporting of raw materials, intermediates, and finished products.Ensure all analytical activities are conducted in line with GMP and ALCOA+ data integrity standards.Utilise a wide range of analytical techniques to support quality control activities.Supervise and mentor laboratory team members, supporting development and performance.Assist with onboarding and training of new starters.Investigate non‑conformances, deviations, and OOS/OOT results, ensuring timely resolution and documentation.Maintain accurate laboratory records and ensure compliance with regulatory requirements.Support continuous improvement initiatives within the laboratory environment.Ensure adherence to all safety, health, environmental, and quality standards at all times.
Essential:
Proven experience in analytical testing within a regulated environment (e.g. pharmaceuticals, medical devices, food manufacturing).Strong understanding of GMP and data integrity principles (ALCOA+).Experience supervising, mentoring, or leading laboratory team members.Ability to investigate and manage non‑conformances and deviations.Excellent attention to detail and organisational skills.A degree in a relevant scientific discipline.You'll be joining a forward‑thinking organisation that places strong emphasis on quality, compliance, collaboration, and continuous improvement, offering an excellent opportunity to progress your career in a senior laboratory position
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