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Are you an experienced Quality Assurance professional looking to take the next step in your career?

Smart4 Sciences is partnering with a growing pharmaceutical manufacturer in Sandwich, Kent, specialising in the production of Cannabidiol (CBD) Active Pharmaceutical Ingredients (APIs) and industrial hemp derivatives for the pharmaceutical and nutraceutical sectors.

They are looking to recruit a QA Officer who will play a key role in maintaining and continuously improving the company's Quality Management System (QMS).

Working closely with Production, Quality Control and the wider business, you'll ensure products are manufactured and released in accordance with GMP standards while supporting a culture of quality and continuous improvement. This is a varied, hands-on role offering exposure across the full Quality Assurance lifecycle, making it an excellent opportunity for someone looking to broaden their experience within a growing pharmaceutical business.

Key Responsibilities:Maintain and continuously improve the Quality Management System (QMS)Review and approve batch manufacturing documentation prior to batch releaseReview and approve SOPs, controlled documents and quality recordsManage Deviations, CAPAs, Change Controls, Complaints and Out of Specification (OOS) investigationsSupport internal, supplier and regulatory auditsAssist with supplier qualification activities and Quality AgreementsSupport product recalls and quality investigations where requiredMaintain GMP training records and ensure compliance across the businessWork collaboratively with Production, QC and other departments to drive continuous quality improvementsSupport validation activities and lead quality improvement initiatives where appropriateWhat We're Looking For:Minimum of 3 years' experience within a GMP pharmaceutical Quality Assurance environmentStrong understanding of GMP and wider GxP regulationsExperience managing QMS activities including CAPAs, Deviations, Change Controls and batch record reviewExperience supporting internal or supplier auditsStrong investigation, root cause analysis and problem-solving skillsExcellent technical writing and documentation skillsGood working knowledge of Microsoft OfficeStrong organisational skills with the ability to manage multiple prioritiesExcellent communication skills and the confidence to work across multiple departmentsDesirable Experience:Validation activitiesSupplier Quality ManagementTraining and mentoring colleaguesContinuous Improvement projectsExperience supporting regulatory inspectionsPersonal Attributes:Highly organised with excellent attention to detailProactive with a continuous improvement mindsetStrong communicator and collaborative team playerAble to take ownership and work independentlyCommitted to maintaining the highest quality and compliance standards

This is an excellent opportunity to join a growing pharmaceutical manufacturer where you'll gain broad exposure across the full Quality Assurance function, take ownership of key quality systems and contribute directly to the company's continued growth and success. If you're looking for a role where you can make a genuine impact while developing your career, we'd love to hear from you.

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