Quality Control Analyst

DCV Technologies Limited ,
Luton, Bedfordshire
Salary: Up to £27,000 per annum + benefits

Overview

Our client is a rapidly expanding player in the pharmaceutical industry that develops, manufactures, distributes and markets a wide range of generic medicine across Europe who have an urgent need for Quality Control Analysts to join them on a permanent basis. Due to the nature of their industry candidates must to come from either a Pharmaceutical or chemical/hazardous background. As it stands, they won’t consider people with a pure FMCG background. Principle responsibilities: · Analysis for the finished product, stability and raw material using HPLC instruments and other wet lab techniques for solid dosage forms. · Followed analysis planning according to the stability schedule and production requirements. · Preparation and submission of the stability reports to the Regulatory, R & D and QA departments for Product Quality Review. · Preparation of the stability schedule, analytical worksheets, validation of the excel sheets for calculation. · Worked with R & D, and Analytical Development team for the New dossier products. · Involved in the MHRA audit and internal audits. · Improving on existing systems and processes where possible. Shifts: · There are 2 shifts for this role which will be worked out on a rota basis. o 7.00am – 3.30pm o 12.00pm – 8.30pm Due to the nature of the business and the working environment, all applicants will be required to fill in a health screening form as part of the application.