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À propos
Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.
This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
This position is responsible for carrying out tasks and projects related to equipment, lab utilities and testing procedures as required by GMP.
Partners with other Departments to ensure that all QC testing activities are completed in an efficient manner.
Duties: Be an active member of the QC group and participates in the following key activities; QC Material Release & Scheduling Activities.
QC Key Performance Indicators.
QC Training
- Personal competency & Team development QC Documentation Review & Approval Site Cross Functional Teams Comply with EHS rules and procedures.
Delivers on the department Goals & Objectives & Continuous Improvement initiatives .
Support relevant internal and external site audits as required.
Maintains and develops knowledge of analytical methods, technology and compliance demands Foster a culture of quality, safety and compliance across the Site Experience and Education: Third level Degree in a science or pharmaceutical discipline.
A minimum of 3 years experience in a quality or compliance role within the pharmaceutical industry. xcfaprz
Significant experience in microbiology within a GMP environment Strong understanding of GMP (Good Manufacturing Practice) Experience with documentation review and approval If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.
Compétences linguistiques
- English
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