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Job Location | Hull |
Education | Not Mentioned |
Salary | Salary negotiable |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Contract , full-time |
PE Global require a QA Analyst to join our Hull facility. This is a diverse and interesting role interacting with all our departments.Description:Compulsory requirementslab/industry experienceQuality lab background desirableattention to detailgood communicatorcomputer literate (microsoft office)1. Job Purpose To perform all activities in compliance with relevant GMP and Quality Systems standards and specifically with FDA Quality System Regulation and ISO 13485. To apply high standards of occupational Health & Safety in the workplace to comply with company policy and procedures. To meet the agreed analysis times and ensure product is released and available for sale in a timely manner with regard to changing priorities. To write under supervision procedures and analytical methods which reflect customer requirements and manufacturing capabilities. Carry out analytical test procedures and work procedures within the work area to ensure maximum safety for themselves and others. Accurately record and report any data generated and submit to the supervisor for verification. To fulfil health safety and environmental obligations and functions set out in their roles and responsibilities section of the HSE Management System. To be involved in the house keeping and calibration of laboratory equipment to ensure day to day performance.3. Job Context / Key Challenges Communicating with a cross-functional team. To collate product information and assist in their review and archiving. To manage a workload which has designated lead times. To contribute ideas to the improved way of working for the laboratories and production areas in compliance with the site procedures. To show initiative in problem solving by identifying and recommending solutions to problems encountered.4. DimensionsThe jobholder works within a team which takes responsibility for all aspects of the QA testing (including development, stability, complaints, competitors and regulatory compliance) of Medical Products and Devices so contributing to the smooth running of thebusiness to ensure standards of customer care are maintained.The team is responsible for maintaining approximately 200 analytical methods and procedures, which control the quality of raw materials through to finished products.5. Knowledge and Experience (Knowledge and experience needed for satisfactoryperformance of the job)6. Organisation Chart (Showing by job title the job holders immediate line manager, peers andsubordinates)Interested candidates should submit an updated CV.Please click the link below to apply, call Miriam on or alternatively send an up to date CV to***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, weare making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you justwant to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in thisadvert.