Jobs, fresher vacancy - Quality Manager • Hampshire

Company: Eurofins UK BioPharma Services

Hampshire

Job DescriptionUnfortunately we are unable to offer sponsorship for this role. 37.5 Hours per week. Monday - Thursday 8.00am - 4.30pm. Friday 7.00am - 3.30pm.Purpose of the post: Working within a small microbiology laboratory, this is a hands on role supporting the operations of the laboratory. A great opportunity for Senior Quality specialist, looking to take the next step of their career.Responsible for the quality management system in compliance with GMPs and company policy. This role will also be required to manage the maintenance of UKAS accreditation.Manage the vendor approval scheme, including sending and collating supplier quality questionnaires and conducting external supplier audits.Manage company validation activities and ensure that all facilities, processes, equipment and methods are fully validated to GMP standards.Maintain the company training matrix and records to ensure compliance.Write, review and amend work instructions, protocols or procedures as appropriate in a timely manner.Ensure compliance with all relevant cGMP, Quality standards and company procedures at all times – this includes reporting any deviations from these standards/procedures.Administer the quality documentation e.g. processing CCRFs in conjunction with the quality systems administratorGenerate a monthly quality report for review at management meetingsPerform self inspection audits in line with the internal auditing programTrack both internal and external audit corrective actions and assist in preparing audit responses.Coordinate and track all calibration activities for equipment to ensure compliance to schedules.Generate quality plans where necessary.Ensure the retention and security of all quality records in conjunction with the quality systems administratorCheck laboratory data, records and log books to ensure they are completed correctly.Investigate unexpected results, errors or problems in methods and offer suitable solutions.Perform data trending and use technical expertise to make suggestions for continuousManage the vendor approval scheme, including supplier quality questionnaires and conducting supplier audits for both suppliers and subcontractors.Responsible for addressing supplier non-conformance issues.Manage company validation activities and ensure that all facilities, processes, equipment and methods are fully validated.Generate, review and approve validation protocols as required.Generate validation protocols or technical reports as required.Maintain the training matrix for the company, ensuring training records are compliant, in conjunction with the quality systems administratorCommunicate with customers, including handling customer enquires; preparing quotations and contract review where necessary.