Total 5 Information Technology job vacancies in Swansea, SA2 8QA

You will be expected to Work with the Network Chair, Lead Clinicians, Health Boards and NHS Trusts, and commissioners, to provide leadership and direction to the work of the network. You will provide leadership and support and produce, analyse and present information that will assist the Network Board in decision-making. At times, this information will cover a variety of organisations and will be highly complex. You will be responsible for organising any associated events and meetings, together with writing and presenting reports for the Network Board. Come and join us in this challenging and rewarding role where your expertise will contribute to the successful delivery of the Vascular Service.

The Recruitment Co are recruiting an experienced Clinical Trials Software Support Engineer to join our clients team. A world-leading manufacturer of high-quality technical products.


Contract: Permanent
Salary: Up to £35,000p.a
Shifts: Full time Days


The Role:
Our client undertakes numerous clinical trials in-house and has developed bespoke software to facilitate this function. This software is used to manage each individual appointment, provide step-by-step guidance on the procedures to be followed along with real-time data collection at each step. The successful candidate will be responsible for maintaining and improving the existing system, providing day-to-day support and ensuring optimal performance and data integrity across numerous clinical suites.


The company has also developed complex image analysis tools that allow quantification of key metrics such as hair counts pre and post treatment. These automated tools are utilised to determine the efficacy of the Companies products using high resolution images captured during the clinical studies. You will be responsible for maintaining, supporting and improving the existing system with a particular focus on ensuring accuracy and integrity of the data.


In addition to direct support of the clinical department, you will be involved in the development of document management systems for the entire business. As the company operates according to numerous International Regulatory Standards, i.e., EU Medical Device Directive and the USA FDA, accurate document control is vital to the ongoing function of the business.
The successful candidate will be heavily involved in the development of a business-wide document management system.


Key Responsibilities:

• Maintain and improve the existing Clinical Trial Software and Hardware system, providing day-to-day support, and ensuring optimal performance and data integrity across numerous clinical suites.

• Further develop our in-house EDC solution allowing integration of various APIs.

• Maintain, support, and improve the existing Image Analysis Software with a particular focus on ensuring accuracy and integrity of the data.

• Maintain and improve, through integration, our separate analytics software package ensuring no commercial restrictions.

• Generate one unified clinical system allowing users to move seamlessly between applications and features from set-up to data delivery.

• Build in key features to enhance performance; EDC, ePRO, eCOA, eConsent, API.

• Safeguard data with robust backup systems, advanced data encryption and audit trails.

• Provide support and infrastructure ensuring maximum performance.

• Ensure documentation is inspection ready. Documentation must meet inspection requirements and must be updated with each release.

• Proactively support the development of a business-wide document management system that captures inputs from design/development/clinical/regulatory and manufacturing departments.

Key Objectives/KPI's:

• Streamline clinical trials making user activities/tasks easier and faster.
• Integrate our EDC solution with ePRO/eCOA and eConsent.
• Design solutions for study set-up, managing multiple sites and user roles.
• Design solutions for ISO information security management certification and FDA 21CRF compliance
• Author software validation documents
• Author Standard Operating Procedures including trouble shooting for the clinical team; correct use of Clinical Trial Management Suite Software, Analytics Software and Analysis Software
• Develop remote access capability for future decentralized clinical trials to improve patient experience

Essential Experience:

• Windows forms applications in VB/C#/.NET including:

• GUI design
• Real-time data collection, manipulation and storage (SQL database)
• Automatic report generation of collated data, primarily direct export to MS Excel
• Image capture and post-processing
• SQL database design, development, implementation and query construction using industry standard tools (SQL Server, Microsoft SQL Server Management)
• Device interfacing via Serial COM, Bluetooth, Wi-Fi etc
• Powershell script development for file management/cloud storage (Sharepoint/Azure)
• Collection of web-based customer data using standard analytics packages
• Maintaining a high level of documentation and validation reports on the tools developed
• Familiarity with Data Protection Rules and Regulations
• App Development

Ideal Experience:

• Managing EDC solution for clinical trials
• Data analysis experience
• Security management and encryption experience
• Hardware and software interface experience

If you have the required skills and experience required for this role then please submit your CV for immediate response.
CPSwansea

The Recruitment Co. is an equal opportunities employer and we're committed to diversity and inclusion in the workplace.

The Recruitment Co. is currently recruiting for a Firmware Engineer (Software) to join our clients team based in the Swansea area.

Contract: Permanent

Salary: Up to £55,000 per annum.

Hours of work: Days / Full time

Location: Swansea

Working alongside engineers from other disciplines and supported by engineering management this role will be responsible for delivering the software platform supporting both medical and consumer IPL beauty therapy devices. Working in a small development team, the jobholder will be required to be comfortable working across the full software design lifecycle, from design through to validation and release. The candidate must be able to effectively communicate the test requirements of their software.
The job holder is expected to have knowledge and experience developing code in line with medical device or other regulated industry standards (MISRA, 60335, 62304, 60601) and be comfortable producing the required associated documentation for regulatory compliance.
The role will be required to deliver work to support a wider product development team, therefore a good work ethic, professional approach to delivery and the ability to communicate issues to a cross functional team is essential. A proven track record of delivery and working understanding of fundamental project and time management processes would benefit the candidate.

Responsibilities:

• Focusing on embedded development for ARM core and Renesas microcontrollers (using C) with some PC side development (primarily in C#) interfacing to the production environment, responsibilities will include:
• Embedded Developing in C & C++ within MISRA guidelines
• Coding with an Object Oriented approach
• Working with Cortex processors especially ST and Renesas parts
• Developing Test Harnesses and Simulators
• Developing code in line with medical device or other regulated industry standards (60335, 62304, 60601)
• PC Based Developing Applications with Visual Studio in C#
• Automation Developing code for control of automated test equipment
• Interfacing to production environment sensors and equipment
• PLC systems and coding

Experience:
Essential

• Use software version control systems (Git, Devops etc)
• Strong C programming skills for embedded platforms (ARM)
• Peripheral communications SPI, UART, I2C
• Experience conducting formal code reviews and working to coding standards
• Strong analytical, problem solving skills to identify bugs and find solutions
• Strong written communication skill for planning and documenting work to meet regulatory requirements
• Familiarity with the software development lifecycle

Desirable:

• Experience working on prototype devices
• Developing with Visual Studio, C++ and C#
• Comfortable working with hardware and electronics (soldering, debugging etc)

If you feel you have the right experience for the above role, please submit your CV for immediate response.
CPSwansea

The Recruitment Co. is an equal opportunities employer and we're committed to diversity and inclusion in the workplace.

You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac.

A Vacancy at Swansea Bay University Health Board.


Responsible for the Health Boards compliance with Environment / Waste Legislation, ISO accreditation and Energy performance.

Working closely with the Technical Services Manager as well as the Estates Department and other Directorates and partners. This role requires a wide range of Environmental knowledge necessitating a multi-disciplinary approach to address the significant challenges faced by the Health Board, therefore applicants should be motivated and enthusiastic with a proven experience of managing within the Environmental discipline.

Regular travel between the Health Board’s large portfolio of sites is an essential requirement of the post.

Working within a small team with in the Estates Department , will be required to interact and provide professional advice to a wide rage of departments within the Health Board.





Lead specialist required to promote of environmental and waste management practices in line with legislation ensuring compliance across ABM University Local Health Board. Provide specialist advice and guidance exchanging complex information as related to waste management where barriers to understanding exist.

Manage the statutory role of Dangerous Goods Safety Advisor, carrying out appropriate audits, developing corrective action plans and producing the statutory annual reports for the Health Board

Work with Health Board Estates Managers to closely monitor and control clinical, hazardous and general waste throughout the Health Board, ensuring strict compliance. Responsible for the specification and subsequent management of all waste management contracted services.

The ability to speak Welsh is desirable for this post; English and/or Welsh speakers are equally welcome to apply.

We believe staff are our best asset and we want you to be happy and confident about starting your career here in Swansea Bay University Health Board.

As one of the biggest healthcare groups in the UK we can offer a wealth of professional training and development opportunities in an innovative, forward-thinking organisation.

You might be a nurse or doctor, maybe you specialise in a health science/therapy or can offer skills in one of our support services - we have a job for you.

There are also apprenticeships, work placements and volunteering roles available.

We are an inclusive employer and welcome applications from everyone whatever their sex; religion or belief; race; age; sexual orientation; gender identity or, whether they are pregnant or have recently been on maternity leave, married or are in a civil partnership; or, whether they are disabled.

Our values - Caring For Each Other, Working Together and Always Improving, show that our commitment to equality is at the heart of everything we do.

If you want excellent career and training opportunities while living on the doorstep of some of Europe's most spectacular scenery, with all the benefits of a thriving and cosmopolitan city - look no further.

You will be able to find a full Job description and Person Specification attached within the supporting documents or please click “Apply now” to view in Trac.




This advert closes on Wednesday 31 Jan 2024

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