• Computer Science Degree
• ISTQB certification
• At least 3 years in QA role
• Experience with test automation tools such as Selenium
• Strong SQL skills
• Experience in an Agile environment

• Competitive Salary
• Healthcare
• Pension
• Remote working flexibility post COVID-19

Senior Automation Tester required for a Dublin based multinational. This is an excellent opportunity for an Senior Automation tester looking to make the transition into a lead role

Salary: Up to €70K with excellent benefits

Responsibilities

• Designing, implementing and maintaining test cases​ based on specifications  
• Engaging in capacity planning, performance analysis and system tuning.
• Executing analysing and reporting on manual/automated test runs
• Lead and manage the existing QA Test team - Coordinating workloads, creating test plans etc
• Supporting the team in whatever capacity necessary to achieve the sprint goal.

Experience

• Solid commercial QA Test experience including in Automation
• Experience working with Java
• Previous Test Lead experience is a plus
• Agile dev environment experience
• API testing
• Multinational / large corporate experience is desirable
• Excellent team player with strong communication skills

*Applicants should hold an EU passport or Stamp4 visa*

Do you want to work for a vibrant, exciting company operating in one of the fastest growing markets online today?

I am working closely with a leading multinational eCommerce company that provide an online marketplace which allows their users to access a vast range of royal-free digital media content.

Currently undergoing a period of growth, I am looking to speak with a talented, passionate and experienced QA Engineer to join this companies Software QA team in Dublin. The perfect candidate will have excellent testing skills, be detail oriented, and will thrive working in a highly technical environment.

This person will work across various teams using a number of tools and technologies and the company are looking for someone with a proven record in enabling the delivery of quality software and engaging throughout the full SDLC.

Duties of the role:

•Interact with PM and Dev teams to gain a strong understanding of the project and the testing objectives.
•Maintain and expand existing testing documentation for product and solutions.
•Work within an Agile environment (using JIRA).
•Protect the overall of quality, security and performance.
•Execute/analyse manual testing and write, execute, and maintain automated tests using the Robot Framework.
•Setup/maintain test environments.
•Support production deployment of applications.

What you need:

•1 - 3 years' experience in QA (at least 1 year to be within an agile environment).
•Excellent understanding of the full Software Development Lifecycle.
•At least 1 years' experience of automated web application test tools (Selenium, Protractor, Robot, etc).
•Knowledge of databases and writing SQL.
•Exposure to/experience in managing frequent releases.
•Excellent communications skills.
•Exposure to PHP, Postgres, Linux implementations (Desirable).
•ISTQB Certification (Desirable).

Please apply at the link provided or contact me for more information on this role and the fantastic package on offer! Call 087 695 0048 or email niall.gormley@stelfox.com

Please note:
We have a number of similar positions currently, and in the future, which we would like to discuss with you should you indicate your interest in this role. When we receive your application for this role, we will contact you to advise you of our process for other similar positions.
Stelfox is fully compliant with GDPR regulations and you can read more in our privacy policy here: https://www.stelfox.com/privacy-policy-gdpr/
Your shared data will not be disclosed or transferred to a third party data controller or data processor located outside the EEA unless we have obtained your express consent.
We look forward to working with you.

Summary:
A Quality Assurance Specialist is required for a pharmaceutical company in South Dublin. The QA Specialist will be responsible for supporting the Quality Responsible Person (QRP) in the implementation, maintenance and ongoing periodic review of the QMS. The QA specialist would support the QRP in the quality oversight of activities conducted in compliance with policies mandatory for all employees, SOPs and regulations and applicable codes of conduct.
Responsibilities:

• Audits & Self-Inspections.
• Training.
• Documentation.
• Product Quality Reviews.
• Product Quality Complaints.
• Deviations.
• Change Management.
• Customer and Supplier Qualification.
• Importation and delivery of products.
• Metrics / Regulatory Compliance.

Qualifications & Experience:

• Degree in technical or scientific disciplines.
• 1 year work experience in an area relevant to the role.
• Report writing, SOP writing, Problem solving.
• Ability to work under pressure and meet reporting deadlines while maintaining an attention to detail.
• Strong interpersonal skills and ability to develop and maintain effective relationships with other departments.
• Quality and compliance mind-set.
• Capable of presenting and reporting to management in an effective manner.
• Self-starter and highly motivated individual.
• Strong team and project management skills.
• Excellent oral and written communication skills.

Summary:
A QA Specialist for Medical Device Combination Product is required for a biotech in West Dublin. The successful candidate will provide quality oversight and support for clinical and commercial devices and combination products from introduction throughout the product and design control lifecycle and the associated Quality System. As a significant quality contributor, the incumbent will proactively engage with all stakeholders involved with supplier quality agreements, device and combination product batch release, risk management and QMS audit preparation during technology transfer and commercial operations.
Responsibilities:

• Responsible for documenting and periodic review of supplier quality requirements and supplier quality agreements.
• Responsible for the review and approval of batch release for combination products.
• Ability to identify non-conforming batch results or trends and escalate them via the Quality Management System.
• Support risk assessments relating to batch release or product quality for clinical and commercial products.
• Ensure timely entry, processing, and closure of quality records in compliance with procedures.
• Support the review of Design Control deliverables including Risk Management activities.
• Responsible for coordination & documentation of the Change Control Review Board for Medical Device Changes.
• Support the development of the QMS as it pertains to Medical Devices and Combination Products to achieve the ISO 13485 standard and compliance with 21CFRPart4 and the medical device regulation 2017/745.
• This will involve supporting quality input to the implementation to the QMS, reviewing new SOPs, mock audits, internal audits and updates to SOPs.
• Support internal audit activity from coordination, preparation and execution to improve the QMS and support stakeholders in adherence to the QMS.
• Supports Notified Body and Health Authority inspections and compliance.

Qualifications & Experience:

• Minimum of a B.Sc. degree in biological /chemical sciences, biomedical/mechanical engineering, or other related subject.
• Minimum of 4+ years’ experience in Quality with medical device or combination products in a regulated environment.
• Risk Management Standard for Medical Devices ISO 14971 2019.
• Knowledge of the regulatory and compliance requirements of design control for medical devices and/or combination products (e.g. FDA QSR 21 CFR Part 4 and 820 / ISO 13485 and Regulation (EU) 2017/745).
• Familiarity with SAP and Trackwise would be desirable.

• Computer Science Degree
• ISTQB certification
• At least 3 years in QA role
• Experience with test automation tools such as Selenium
• Strong SQL skills
• Experience in an Agile environment

• Competitive Salary
• Healthcare
• Pension
• Remote working flexibility post COVID-19