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Supply Quality Specialist - Multinational Pharmaceutical Company / Wales
This job has expired or may no longer be taking applications, but other similar jobs are available.
Added: | 2019-06-19 |
Location: | Wrexham, Wales |
Salary: | £35000 - £40000 per annum |
Duration: | Permanent |
Apjid | 3 |
Supply Quality Specialist – Wrexham - £35,000 - £40,000
An expanding multinational Pharmaceutical company who are one of the largest generic Pharmaceutical manufacturers in the UK are looking to appoint a Supply Quality Specialist to their Quality department to add to their 350 strong work force (8,000 worldwide).
As the Supply Quality Specialist your role will be to ensure that products are manufactured and processed in accordance with company, corporate and international standards with respect to cGMP, product safety, quality and efficacy.
You will ensure that current industry standards are applied to the transfer of CP Pharmaceutical such as described in the ISPE Good Practice Guides for technology transfer and operations management. You will also be required to ensure that the requirements of GAMP and equivalent standards are applied as appropriate with third party suppliers.
Ideally I am looking to speak with Quality Specialists with experience from a Pharmaceutical background and knowledge of the current industry standards for technology/product transfer as given in current regulations and guides such as the ISPE good practice guides. Educated to degree level in a scientific discipline.
An expanding multinational Pharmaceutical company who are one of the largest generic Pharmaceutical manufacturers in the UK are looking to appoint a Supply Quality Specialist to their Quality department to add to their 350 strong work force (8,000 worldwide).
As the Supply Quality Specialist your role will be to ensure that products are manufactured and processed in accordance with company, corporate and international standards with respect to cGMP, product safety, quality and efficacy.
You will ensure that current industry standards are applied to the transfer of CP Pharmaceutical such as described in the ISPE Good Practice Guides for technology transfer and operations management. You will also be required to ensure that the requirements of GAMP and equivalent standards are applied as appropriate with third party suppliers.
Ideally I am looking to speak with Quality Specialists with experience from a Pharmaceutical background and knowledge of the current industry standards for technology/product transfer as given in current regulations and guides such as the ISPE good practice guides. Educated to degree level in a scientific discipline.
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