Quality Analyst

4 weeks ago

Cheshire, United Kingdom Manpower Full time

Manpower has a great opportunity for a Temporary Quality Analyst Role within a pharmaceutical environment available in Holmes Chapel.

This role provides testing, reporting and investigation laboratory activities to enable compliant, on time delivery of product to market. This is a key position within a QC team ensuring that the exacting standards of GMP, Site procedures, HSE and LEAN arealways delivered

End Date - End of September 2023

Shift - 5D2 (6am-2pm / 2pm-10pm)

Base pay rate - £13.68

The individual should have a good understanding of analytical chemistry or microbiology, laboratory instrumentation and/or related information systems and a science degree / HND/ NVQ 4 or equivalent with at least 1 years working experience in a GMP environment

**Experience and Requirements**

? Computer-literate with experience in the use of Laboratory (LIMS, Data capture) systems as well as MS Word, Excel and PowerPoint

? Demonstrated ability to actively participate in projects and investigation

? Knowledge and understanding of global pharmaceutical regulations and guidelines.

? Demonstrates competence and clarity in both written and oral communication e.g. presentations at team meetings, ability to write ILIs and demonstrates understanding to execute FSIs as well as non-complex technical and investigational reports, communicationat team meeting

? Good interpersonal skills with an ability to communicate procedures and concepts within the team and on occasions to the department. Ability to train instructional techniques

? Self-motivated with ability to plan and manage own workload with some supervision during the working day.

? Challenges and questions locally and across team ways of working to seek improved processes and performance

? Takes responsibility for supporting change, is prepared to take or support action, and/or escalate to ensure implementation of appropriate actions

? Ability to respond to auditor questions and describing local systems on external audit tours with positive outcomes

? The individual should have good knowledge and understanding of the principles and concepts of compliance management and GMP/GLP

? The individual should have a basic understanding of the industry and be responsive to of regulatory changes, new technologies, Pharmacopoeia requirements and their impact on the function.

? An understanding of own quality assurance function, as well as a basic understanding of other

functions and how they contribute to achieving the objectives of the business.

? The individual has some understanding of business functions and supports reacting to issues on how QC performance impacts functional customer service.

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