Job Description
Quality Control Analyst
Department: Quality
Location: Waterlooville, Hampshire (on-site)
Reports To: Head of Quality
Employment Type: Full-time
Job Summary
We are seeking a Quality Control Analyst to join our expanding Quality team. The role involves conducting routine physiochemical and organoleptic testing on various products, manufactured bulks, and raw materials. The analyst will investigate non-conformances, manage standard libraries, and maintain lab organization. The ideal candidate will have knowledge of analytical testing techniques, strong scientific report writing skills, and the ability to collaborate cross-functionally to improve product quality, compliance, and operational efficiency. This position offers an opportunity to learn detailed product knowledge about cosmetics manufacturing and to drive quality excellence in a fast-paced, regulated environment.
Key Responsibilities:
* Conduct physiochemical and organoleptic testing on manufactured bulk, raw materials, and finished goods to ensure compliance with specifications, including FTIR, viscosity, odour, appearance, and texture testing.
* Perform experimental work independently following SOPs and test methods.
* Investigate non-conformances and assist with deviations, CAPAs, and change controls.
* Maintain lab cleanliness, manage reagent stocks, perform equipment checks, and manage standard libraries.
* Assist in maintaining controlled documentation, SOPs, and records according to quality standards.
* Collaborate with other departments such as Manufacturing and Production to ensure product quality and compliance.
* Lead training programs for junior analysts and manufacturing operators.
* Promote a culture of Quality and Continuous Improvement across the company.
Experience and Qualifications:
* BSc in a relevant scientific field or equivalent experience.
* Previous experience in a QC Laboratory or similar role, ideally within the Cosmetics or regulated industry.
* Strong olfactory differentiation skills are preferred.
* Experience with LIMS or GMP record-keeping is desirable.
* Knowledge of quality standards such as ISO 22716 and GMP requirements.
* Understanding of DI principles and their impact on laboratory work.
* Excellent scientific report writing, problem-solving, and attention to detail skills.
* Strong communication and influencing skills across departments.
* Experience with Root Cause Analysis tools (e.g., 5 Whys, Fishbone).
* Passion for quality and fostering a quality mindset in others.
#J-18808-Ljbffr