Senior Quality Control Analyst

Position Overview An experienced and detail-oriented Quality Control Senior Analyst is sought to join a pharmaceutical manufacturing facility specialising in the development and production of medicinal products. The role involves performing laboratory testing, supporting analytical method validation, and ensuring compliance with Good Manufacturing Practice (GMP) and quality standards.

Key Responsibilities
Reporting to the Quality Control Manager, the selected candidate will perform sampling and analytical testing of raw materials, packaging materials, work-in-progress products, finished goods, and stability samples. The role includes participating in analytical method development, validation, and laboratory transfer activities, preparing validation reports, and reviewing analytical documentation in accordance with current Good Laboratory Practice (cGLP). Responsibilities also involve maintaining laboratory cleanliness, monitoring environmental conditions, and ensuring compliance with GMP regulations, including EudraLex Volume 4 guidelines. The candidate will ensure sample traceability, accurate documentation, and adherence to safety and security procedures, particularly when handling controlled substances. Additional responsibilities include monitoring analytical techniques used by other QC Analysts, providing guidance, and supporting continuous improvement within the laboratory. Requirements Candidates should hold a degree in Chemistry, Biology, Medical Laboratory Science, or a related scientific discipline. Applicants with a BTEC National Diploma in Applied Science will also be considered. A minimum of 2 years of experience in a Quality Control Chemistry Laboratory, or an appropriate combination of education and experience, is required. Strong knowledge of analytical testing, laboratory equipment operation, troubleshooting, and chromatographic techniques, particularly HPLC and GC, is essential. Previous experience in analytical method validation will be considered an advantage. The ideal candidate should demonstrate excellent time management, organisational, teamwork, and communication skills, together with proficiency in Microsoft Office applications. Applicants must be able to communicate effectively in written and spoken English and possess a valid EU working visa. What’s Offered The position offers a minimum annual salary of €30,000, depending on qualifications and experience, together with flexible

working hours
within a single-shift structure. The successful candidate will benefit from professional development opportunities within a regulated pharmaceutical environment, including the opportunity to gain practical experience in the medicinal cannabis industry.