Job Overview

Apply now 3R Consulting are recruiting a Production Supervisor for a leading contract pharmaceutical company working with global customers to develop new pharmaceutical and biotechnology products. You will be responsible for co-ordination of manufacturing and warehouse activities (man management planning/execution & reporting) within the production facility. You will co-ordinate and prioritise the activities of support functions including raw materials testing, QC testing and QA support. You will produce production schedules, generation & approval of batch documentation ensuring compliance with the quality management system and associated CAPA, receipt of orders, stock management and measuring area performance and supporting audits. You will have excellent organisational & communication skills ensuring efficient running of the department. You will be experienced in leading teams, planning production schedules, maintaining stock control systems and producing /approving documentation to GMP standards. Salary £negotiable + Benefits To apply for the position please forward your CV to the recruiter below:

Key Requirements

CAPA GMP Management Reporting Production Schedules