degree in scientific or engineering discipline
background in pharmaceutical GMP manufacturing
About Our Client
A global pharmaceutical business with the highest commitment towards product quality and patient care. The business have GMP manufacturing sites across the world and offer excellent opportunities for their staff.
The validation specialist will lead and perform small to medium size validation activities including improvement activities and major projects ensuring that resources, raw materials and documentation are available to facilitate the smooth running of validation activities. You will coordinate and perform validation activities and track the progress to QA and process leaders. Your role will be critical in maitaining validated status and provide technical leadership on validation activities.
The Successful Applicant
The ideal candidate is likely to be a graduate or be able to demonstrate academic potential to this level and have experience working in a pharmaceutical environment. The role holder must have well developed interpersonal and communication skills to achieve success in their role. Time management, diplomacy, assertiveness, leadership skills and the ability to work under pressure are also essential.
What's on Offer
Initial long-term temporary contract
Competitive hourly rate
Opportunity of further employment
Opportunity to work with the best people in their field.