Location
North West London, NW2 7HF

Hours
Monday – Friday 9:00am – 6:00pm with 1 hour lunch break

Salary
Competitive

Work Arrangement
Hybrid: 3 days in office, 2 days working from home

About the Role
Are you detail-oriented, committed to maintaining high standards, and passionate about delivering quality? We are seeking a proactive and organised Quality Control Officer to join our team at Vitabiotics. In this role, you will play a key part in ensuring our products, processes, and services consistently meet regulatory requirements, company standards, and customer expectations. Working collaboratively across departments, you will help drive continuous improvement, identify opportunities to enhance quality, and contribute to maintaining a culture of excellence throughout the organisation.

Your responsibilities will include reviewing analytical, microbiological, and physical test results for raw materials, bulk products, and finished goods; evaluating test data against approved specifications; participating in investigations relating to out-of-specification and atypical results; reviewing bulk product samples and manufacturing documentation; managing stability programmes including data review and reporting; generating and verifying Certificates of Analysis; releasing raw materials after quality assessment; ensuring compliance with GMP, HACCP, and food supplement regulations; supporting audits and investigations; and contributing to continuous improvement initiatives and quality metrics reporting.

Vitabiotics is a pioneering company in nutritional healthcare products with over 50 years of innovation, exporting to over 100 countries and recognised for its clinical research excellence. Join a diverse and talented team that values innovation, mutual respect, teamwork, and commitment.

Qualifications
Degree or equivalent qualification in Chemistry, Pharmaceutical Science, Microbiology, Food Science, Biology, or a related discipline.

Experience
Experience working within a pharmaceutical, nutraceutical, food supplement, or regulated manufacturing environment.
Understanding of GMP and quality management systems.
Experience reviewing analytical data and quality documentation.

Desirable
Knowledge of HACCP and food supplement regulations.
Experience generating Certificates of Analysis and batch release documentation.