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Job Location | Macclesfield |
Education | Not Mentioned |
Salary | Competitive salary |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent, full-time |
Would you like to apply your expertise to impact of Sterilisation in a company that follows the science and turns ideas into life changing medicines Then AstraZeneca might be the one for you!At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible. Every one of our employees makes a difference to patient lives every single day. In these roles, you can be a part of this by ensuring your customers can focus on delivery of novel lifesaving medicines, as you assist them to administer their complex business lives.We are offering this new and exciting progressive role to support sterile manufacturing facilities at our Macclesfield campus. The campus supplies products for most of the AstraZeneca therapy areas to global markets and thus has long term development opportunities.Sterilisation processes that youll be involved in include steam/dry heat sterilisation.Well ask you to support and run a schedule of steriliser qualifications for your assigned Manufacturing Plants, processing facility and for the Quality Assurance Department. This is comprised of 18 units including autoclaves, sterilising ovens and freeze dryers. On a periodic basis, the sterilisers undergo qualification testing in order to validate and verify that they are performing consistently. Your remit will be to ensure that this work is completed in a timely manner whilst minimising the loss of production time.Youll be working within a team to achieve operational delivery within a complex or multidisciplinary production environment.Youll assist in drafting the appropriate qualification programmes and the associated reports to meets the standards required by the relevant works and regulatory authorities.You will contribute to running qualification cycles by placing Biological indicators and Thermocouples in predefined locations as per qualification programmes.By supporting the problem solving and correction of problems associated with sterilisation issues, youll contribute to improving the efficiencies of the manufacturing operation.Well support you to assist in implement of new equipment, systems and procedures. This will assist us in meeting increasing demand from business and/or regulatory standards aimed at providing higher levels of sterility assurance.Well encourage you actively support in any ongoing continuous improvement project. This will develop your personal lean/manufacturing excellence knowledge.Working closely within your business area and other aligned support services, youll participate with continuous improvement activities or projects so that they meet the agreed objectives.Well give you the opportunity to support formal and informal training of less experienced staff and new starters to meet the line and business requirements. Essential Requirements: