Document Control Officer in Runcorn

Would you be interested in joining a global healthcare company that specialises in lifesaving medicines and technologies for infusion, transfusion, and clinical nutrition? Are you driven and highly motivated with the ability to help drive and improve business performance? Do you have a good knowledge and understanding of cGMP? If you’ve answered yes, then read on to find out how you could be involved in driving the next major project and get in touch now to avoid missing out! The opportunity Given increased project expansion, a fantastic opportunity has opened  to have the chance of joining a well-established UK business located in Runcorn as an Document Control Officer. Working Shifts 7am - 3pm and 3pm - 11pm. The role As a Document Control Officer, you will ensure to achieve high standards of productivity and to ensure that all documentation generation and checking meets cGMP requirements. This role will be Contract based- 5 months with potential for extension. Your duties and responsibilities will be Ensure all documentation is generated in a timely manner to meet production plan. Generate batch documentation and labels required to produce all items in line with the production plan. Complete and check the necessary calculations required on batch documents. Confirm that information on batch documents and labels corresponds to master documents/formulations. Complete any other administrative and clerical duties required under Good Manufacturing Practice. Responsible for required activities necessary to meet the prescribed production schedule. Ensure compliance with cGMP and all relevant legislation & company policies & procedures including but not limited to, Health and Safety, MHRA Guidelines, ISO standards and the requirements of the Quality Management System (QMS). Assist with investigation into failures and ensure that all documentation associated with the QMS (Quality Management system) is completed accurately and in a timely manner eg: Deviations, Change Controls and Environmental Excursion reports. Delivery of the compounding unit’s objectives and targets within the defined time frames. Satisfactory internal and external audit management to maintain full accreditation. Ensure all documentation is readily available and prepared in time for the required production day. Reliability of attendance/timekeeping Completion of ALL written records. Training Compliance of ALL personnel (SOP’s). Contribution to and delivery of team’s work plan Undertake training as requested.Personal Attributes High accuracy and clear documentation writing. Driven and highly motivated. Flexibility Good organisational and planning skills Desire to continuously improve business performance. Computer literate. Excellent communication and interpersonal skills. It’s great if you also have the following Pharmaceutical manufacturing experience preferred.Get in touch now If you're on the lookout for a new opportunity, where you will ensure successful documentation is carried out to help drive key projects, then this could be the role for you so apply now to avoid this fantatsic opportunity! Millbank Holdings Ltd is an equal opportunities employer and respects diversity. We welcome applications from all suitably qualified persons who are eligible to live and work in the UK. Millbank is proud to be a member of the ‘Disability Confident Scheme’. Millbank operates as an Employment Agency and Business