Software Quality Engineer

Software Quality Assurance Specialist - International Pharmaceutical - £40,000 East Anglia

SUMMARY
There is now the opportunity for an experience Quality Software Engineer to join an international Pharmaceutical Company providing quality assurance expertise and facilitation to the Quality department. You will be working within an organisation who believes strongly in employee development and progression in a senior position that will see you behind some important decisions for driving the company forward.

JOB TITLE: Software Quality Assurance Specialist / Computer Systems Validation / Software Quality Engineer / CSV

LOCATION: Southeast, East Anglia, Cambridgeshire, Bedfordshire, Hertfordshire, London

COMPANY STATEMENT: This is an international pharmaceutical company who specialise in a number of market leading niche products. They have been growing continually and are at the forefront of their field. They are looking for bright, enthusiastic and innovative individuals who will grow and develop with the company.


BENEFITS: Salary, bonus, pension, healthcare, life assurance and excellent training and career progression.


ROLE/DESCRIPTION:
This role will be based within research & development projects and will also be required to provide Software Quality Assurance support to other projects or areas within the business such as Quality System Computer System Validation and laboratory equipment computerised systems validation. All these elements are essential to be successful within this role.

You will be;

- assisting the various design & development project teams with both embedded device software qualification and supporting computer system validation
- supporting development and roll out of any identified software design lifecycle processes
- identifying any Software Quality Assurance training needs within the project/quality team, and execute training
- giving final approval of each stage of Quality Assurance lifecycles to ensure all required processes and regulations have been adhered to
- planning, coordinating and executing validation activities in line with the CSVMP and site software SLC procedures
- ensuring that the relevant software risk management documentation is up to date and adequately reflects the direction of the project and any changes that may be required during development


REQUIREMENTS:
- Experience of embedded software



ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com


TO APPLY

If you would like to discuss this vacancy further, please call Principal Consultant Stephen McAnaney on +44 (0)20 3189 2299, or email smcananey@i-pharmconsulting.com. If this role is not suitable, Stephen is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


KEY WORDS:

Quality Software Engineer, Computer Systems Validation, Software Engineer, CSV, CSVMP, Compliance, Quality Assurance, Project Management