Quality Assurance Functional Test Engineer – NTT DATA
We are seeking an experienced Quality Assurance Functional Test Engineer to join our team. This person will provide quality assurance testing for corporate banking applications to ensure any business‑requested changes are validated prior to handing off to UAT. You will learn the business as well as understand the testing framework and processes for the applications.
Your responsibilities include developing solutions to automate test processes, designing maintenance procedures and documentation, automating repetitive steps in workflows, and collaborating within an open and collaborative approach to work on solutions for applications and workflow processes.
7–9 years of experience in QA functional testing.
Experience in corporate banking domain/applications.
Conversant in ITIL.
Prepare automation strategy, plan and develop data reconciliation automations.
Experience designing frameworks.
Good knowledge of automation testing tools.
Experience with defect management tools such as QC or Jira.
Hands‑on experience with databases, data warehouses (ETL), data conversion, data migration, functional/regression, back‑end/front‑end, and API testing.
Leadership in driving QA projects.
Playwright experience is an added advantage.
NTT DATA is a $30 billion trusted global innovator of business and technology services. We serve 75 % of the Fortune Global 100 and are committed to helping clients innovate, optimize and transform for long‑term success. As a Global Top Employer, we have diverse experts in more than 50 countries and a robust partner ecosystem of established and start‑up companies. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure and connectivity.
NTT DATA is an equal opportunity employer.
Senior Quality Engineer – Manufacturing (Stryker)
Join our team as a Senior Quality Engineer and work in one of our busiest manufacturing facilities in a role that blends project‑focused work with operational support. This position will work cross‑functionally and across multiple sites to ensure the highest quality standards are met.
Work within the quality operations team under minimal supervision.
Work closely with operations and business functions to ensure quality performance of product and processes.
Oversee and approve NC & CAPA, activist and mentor in problem solving and root‑causing activities.
Lead and participate in the development and improvement of manufacturing processes for existing and new products.
Analyse and review concession requests.
Review and approval of change management activities.
Maintain KPI for monitoring process quality, perform analysis and interpret trends, take action as necessary.
Support execution and analysis of QATs.
Advocate Human Factor practices, proficient in the science of Human Factor identification and mitigation.
Develop and provide input for risk management by identifying opportunities and weaknesses.
Participate and interface in internal & external audits with regulatory representatives, providing effective narrative and description of topic of expertise.
Assist in the development, responsible for review & approval of process and equipment validation/qualification.
Support manufacturing transfers to other plants/facilities, leading quality activities.
Coach and mentor others in quality topics and activities.
Bachelor of Science or engineering.
Minimum 2 years’ experience in an engineering or science‑based position.
High level of PC skills – proficient with Microsoft Word, Excel and PowerPoint.
Self‑starter with efficient work style and ability to handle multiple tasks in a fast‑paced environment.
Willing to work as part of a multi‑site team, with some travel required.
Knowledge of risk‑based and statistical concepts desirable.
Problem solving and analytical skills.
Builds strong relationships by fostering open communications, respect and trust. Strong team player and acts with a customer service/stakeholder focused approach.
Diplomatic, tactful and leverages excellent interpersonal keys to help achieve outcomes.
Accepts change openly and adopts a continuous improvement orientation.
Excellent English (both oral and written).
Ability to be the voice of quality when dealing cross‑functionally.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.
Quality Engineer I – Medical Devices – Pale Blue Dot (Galway)
Our client, a dynamic and fast‑paced medical device start‑up based in Galway, is seeking a Quality Engineer I to join their growing team. The company focuses on developing innovative, patient‑centric technologies to improve quality of life and is advancing rapidly through the product development lifecycle toward global market launch.
Responsibilities include but are not limited to the following:
Apply quality engineering expertise across the Quality Management System (QMS).
Support certification and maintenance of compliance to ISO 13485 and 21 CFR Part 820.
Assist with design assurance activities, including design controls, verification, and validation.
Support development and validation of test methods and computer system assurance programs.
Participate in risk management and usability engineering activities.
Maintain document control through QT9 eQMS and perform related administrative tasks.
Contribute to CAPA and non‑conformance investigation and resolution process.
Assist in internal and external audits and implement corrective actions as needed.
Support updates and gap assessments for applicable regulatory standards and guidance.
Participate in supplier quality management, vendor evaluation, and AVL maintenance.
Collaborate cross‑functionally to uphold quality objectives and continuous improvement.
Perform additional quality‑related duties to support business goals and KPIs.
Bachelor’s degree in engineering, science, or related field (or equivalent).
Minimum of 2 years’ experience in a medical device or supplier environment.
Familiarity with ISO 13485, FDA QSR (21 CFR Part 820), and GMP requirements.
Experience in both FDA and European regulatory environments is preferred.
Strong initiative, problem‑solving, and follow‑through in executing responsibilities.
Understanding of risk management methodologies (ISO 14971).
Experience with sterilization (EtO/Gamma), biocompatibility, and transportation testing is a plus.
Prior involvement in audits or inspections is an advantage.
Proficiency in MS Office and familiarity with electronic QMS tools.
Immediate interviews available for suitable candidates.
#J-18808-Ljbffr