Quality Control Analyst

3 weeks ago

Cheshire, United Kingdom Experis LTD Full time

**Quality Control Analyst x 3**
**Holmes Chapel**
**5 Months**
**£12.31 - 15.13p/h PAYE (Dependant on Experience)**
**Role Brief**:
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 aredelivered at all times.

**Key Accountabilities**:
? Coordinates & conducts testing of analytical samples for the specific laboratory area.
? Analyse complex data, introduce use of statistical tools
? Contribute to quality key performance indicators and deliver measure/trend data to team. Challenge and seek improvements in ways of working/processes and put actions in place
? Acts as assistant to the QC Team Leader support work prioritisation, organisation and
improvement.
? Deputises for the Team Leader when needed
? Acts as a Technical expert within the team with ability to support internal, Global regulatory inspections and customer audits.
? Delivers key training and support to other QC team members in the delivery of their roles
? Leads investigations (i.e. Events/ILI/FSI/PPS), working primarily within their local area and cross
functionally where required, to problem solve, identify root cause and implement meaningful
CAPA.
? Leads change activities to deliver improvement activities, support business process improvement and continuous improvement (e.g. LEAN)
? Evaluates analytical methods and compendia to define the operational laboratory processes to
ensure compliance and efficiency in a QC environment for both GMP and HSE considerations
? May be required to front area of expertise during regulatory inspections and customer audits

**Skills Required**:
High level of technical knowledge and expertise of quality control principles and systems in a GMP
environment.
? Computer-literate with experience in the use of Laboratory (LIMS, Data capture) and some Quality
(Deviation, Change Control, CAPA support, Documentation) systems, an understanding of
Statistical analysis packages as well as MS Word, Excel and PowerPoint
? Demonstrated ability to lead and deliver projects and investigations over short timescales (i.e. up
to 3 months)
? Demonstrated knowledge and understanding of global pharmaceutical regulations and guidelines
and ability to support reviews.

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