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Quality Systems Administrator

Employer
Vectura
Location
SN14 6FH, Chippenham
Salary
Competitive base plus comprehensive benefits including annual bonus and pension
Start date
13 Apr 2019
Closing date
13 May 2019

View more

Discipline
Quality
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job summary

This is your opportunity to use your quality mind-set and excellent IT skills to support and continuously improve Vectura’s paper and electronic document systems. Your knowledge and experience will ensure all controlled documents meet internal/external requirements and support our mission to have a positive impact on patients’ lives around the world.

What you get

In return for your skills and expertise, we offer a competitive base salary, annual bonus and generous benefits package including a pension plan, life assurance, private health, dental plan, share save/incentive schemes, cycle to work scheme and free parking. – To find out more or to apply click the ‘Apply’ button.

Your role

Working within the Quality department, you’ll be an advocate for embedding a ‘culture of quality’ across Vectura. You’ll provide controlled document system expertise to facilitate maintenance and continual improvement of Vectura’s paper and electronic document systems. You’ll use your IT skills to act as systems administrator for our electronic document systems and training management system.

Other key responsibilities will include (but not limited to):

·Management of the on and off-site archive facilities to ensure control of Quality and project documentation and records

·Generate KPIs for the Quality Management System

·Generate and maintain relevant SOPs and other documentation

·Provide guidance and support to colleagues on company document systems

·Support company infrastructure projects relevant to the role

·Maintain a basic understanding of the applicable GMP/ISO requirements

What you need

You’ll be educated to A Level standard or equivalent with demonstrable experience working with electronic document management, control and archiving. Preferably with experience of working in a regulated industry sector, you’ll possess a basic understanding of applicable GMP/ISO requirements. You’ll be highly computer literate, including MS Office applications, be an excellent communicator and highly organised with proven high attention to detail.

About Vectura

We’re global leaders in the development of innovative formulations and devices for inhaled medical products. Working collaboratively, we combine technical, engineering, clinical and regulatory expertise to design, develop, industrialise and deliver a unique range of innovative products, from smart nebuliser technologies to innovative formulations.

With a healthy pipeline of new products in development, as well as partnerships with major international pharma companies, our Quality department is expanding to meet the challenge. Join us and you’ll find it’s an ideal place to develop a stimulating and rewarding engineering career.

Apply

If you’re interest and wish to apply or find out more information about Vectura and the role please click apply. Closing date for applications is 04 March 2019

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