Quality/Validation Project Leader

Description

I am currently recruiting for a Quality/Validation Project Lead on a CONTRACT basis for a client of mine based in South West London for a Leading Pharmaceutical and Healthcare company. They are looking for someone to ideally have experience in:

Management of the Master Validation Plan

Write and/or review DQ,IQ,OQ,PQ of equipment and process validation protocols and report

Cleaning validation.

Liaise with Quality to complete CAPA and Deviation reports.

Contribute to any team working on New Product Introductions.

Take part in monthly site inspections and internal audits as required.

FDA

Corrective Actions

- Strong Project Management skills and able to lead and manage ~6 technical specialists

- Pharma Quality background. Understand QMS requirements to meet FDA Regulations.

- Good communication and reporting skills

- Experience of change management in a regulated environment

Contract Length: 8 -12 Months

Start: ASAP

Location: South West London

If you are looking for your next position and feel like this would suit your skill set please send a copy of your updated CV and I will be in touch. Alternatively if you know someone who would be great for this do pass the details on.

To find out more about Huxley Engineering, please visit www.huxleyengineering.com

Huxley, a trading division of SThree Partnership LLP | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales