Job Vacancy Senior Micro QC Analyst with Ck Science

Senior Micro QC Analyst - Ref: ST16411
Company: Ck Science
Contact Name: Jason Johal
Salary: £21000 to 31000
Employment type: Full Time
Post Date: 23/07/2008
Job Location: Cambridgeshire - Anglia-Cambridgeshire - England
Job Category: Science  [ View All Science Jobs ]
 
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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.
 
Other Information

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.
Degree:
Experience (year): Unspecified
 
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