My Client a World Leading Med Device/Wound Care company has opened up excellent opportunities in their QA Laboratory Team, they are looking for Senior QA Analysts to join their team on a fixed term contract basis at there offices in East Yorkshire

Core Responsibilities:
•To support and provide job training and supervision for the lab team in the ways of working.
•To manage the planning, performance, reporting, evaluation and authorisation of work activities and products, in conjunction with the Team Leader, to enable the meeting of agreed analysis times and ensure product is released and available for sale in a timely manner with regard to changing priorities to ensure that internal and external customer requirements are met.
•To investigate and report defects arising from customer complaints, deviations and non-conformances and track the agreed actions so recurrence is prevented.
•To write procedures and analytical methods which reflect customer requirements and manufacturing capabilities and take account of Smith & Nephew requirements with respect to their suppliers.
•Assist in the supervision of a sub-section of the QA laboratories at levels up to Senior QA Analyst participating in training and development of junior personnel to ensure technical output is of a consistent high quality.
•Ensure analytical test procedures and work procedures within the work area are performed considering maximum safety for their self and others.
•Write technical reports, regarding work involving non-standard procedures and technical complexity, sometimes involving numerous parameters so that information can be provided to other departments.
•To fulfil health safety and environmental obligations and functions set out in their roles and responsibilities section of the HSE Management System.
•To be involved in the house keeping and calibration of laboratory equipment to ensure day to day performance.
•To perform all activities in compliance with relevant GMP and Quality Systems standards and specifically with FDA Quality System Regulation and ISO 13485.

Key Skills/ Experiences:
•A BTEC or equivalent degree science subject (2 (ii) honours), preferably in Microbiology or Chemistry
•At least 3 years experience within QA
•experience in HPLC, Chromatography, Medical Devices and Tensile Testing would be desirable
•Good interpersonal skills are essential


My client has a fantastic reputation within the industry and is well known for looking after there employees. The hourly rate/salary for this position is dependant on experience. 




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