QC /QA Analysts – contract / temporary

Kingston Upon Hull
£13 - £17/hour
22 Jul 2017
21 Aug 2017
Contract Type
Full Time
INTERIM/contract role on an hourly rate

Our client is a world leader in health and hygiene; a global company with a large state-of-the-art manufacturing facility in Hull. As a result of business expansion, there are immediate requirements for QC Analysts to START IMMEDIATELY !!!!! on a temporary basis

Your role:

* Stability and release testing of products in compliance with cGMP

* Analysis to support key site validation activities in compliance with cGMP

* Maintenance of analytical equipment - Maintaining laboratory records to current cGMP requirements

* Accountable and responsible for analytical and quality system\support related tasks relating to the QC area

* The QC Analyst is responsible for ensuring that they deliver their output effectively and efficiently in compliance with GLP practice

* Day to day execution of analytical testing in conformance with all relevant safety and quality requirements

* To ensure that relevant data is checked, approved, recorded and available for inspection in accordance with Good Manufacturing & Control Laboratory Practices

Essential Skills:

* Able to work alone with minimal supervision
* Recent experience in HPLC and / or GC
* Able to demonstrate good written and verbal communication
* Able to make most efficient uses of resources and ensure deadlines are met

Key responsibilities of the Quality Control Analyst are:

* Adhering to the principles of GMP including good documentation practices.

* Managing the performance of and training junior lab personnel, reviewing their workload and driving development.

* Performing analysis using HPLC, GC, UV and IR

The ideal candidate for the Quality Control Analyst:

* Will have a BSc ideally or equivalent in a Chemistry degree, if not experience in analytical lab environment

* Must have previous experience with HPLC, GC, wet chemistry techniques, UV and IR.

* Must have experience testing pharmaceutical products in a GMP environment

* Experience of testing finished products (any formulation type)
* Experience in hands-on HPLC analysis, Chromeleon experience preferred