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| I am looking for a senior analyst to be responsible for activities relating to the analysis of all microbiological testing and release activities on my clients' site. You will have specific technical expertise in Quality Control operation and will lead investigations to identify root causes and the appropriate preventative actions. You will design and deliver training on microbiological techniques and provide technical support to the team and will review analytical raw data generated by group, ensuring compliance with cGMP. As part of the role you will be expected to deputise for Analytical Team Leader as and when required and you may be required to perform validation of analytical methods, qualification of equipment and transfer methodology to and from other groups. It is essential that you have a significant understanding of the pharmaceutical regulatory process and a proven, sustained competence in analytical techniques and skills relevant to the role. Entitlement to work in the EEA is required. Please quote reference ST16411 in all correspondence. | ||||||||||||||||
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| Skills: | I am looking for a senior analyst to be responsible for activities relating to the analysis of all microbiological testing and release activities on my clients' site. You will have specific technical expertise in Quality Control operation and will lead investigations to identify root causes and the appropriate preventative actions. You will design and deliver training on microbiological techniques and provide technical support to the team and will review analytical raw data generated by group, ensuring compliance with cGMP. As part of the role you will be expected to deputise for Analytical Team Leader as and when required and you may be required to perform validation of analytical methods, qualification of equipment and transfer methodology to and from other groups. It is essential that you have a significant understanding of the pharmaceutical regulatory process and a proven, sustained competence in analytical techniques and skills relevant to the role. Entitlement to work in the EEA is required. Please quote reference ST16411 in all correspondence. | |||||||||||||||
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| Experience (year): | Unspecified | |||||||||||||||