Senior Quality Assurance Engineer

We’re looking for a **Senior QA Engineer** to join our team. As a Senior QA Engineer, you will be responsible for leading the quality assurance effort for our products. You will be reporting to the Director of Quality and Regulatory Affairs and working closely with our development team to ensure that our platform meets the highest quality standards. If you are a detail-oriented problem solver with a passion for quality, we want to hear from you

QMENTA is a multi-disciplinary science and engineering start-up. The company’s mission is to develop technologies to better understand the healthy and diseased brain. We are a fast-growing startup. In the last 9 years, we have expanded our business globally and served hospitals, research centres and pharmaceutical companies in the US, Europe and Asia-Pacific.

As we embark on this exciting new chapter of growth, we're thrilled to share that our company is well-funded, enabling us to explore innovative avenues and expand our impact. This significant support underscores our commitment to pushing boundaries and achieving new milestones, propelling us forward in this exciting journey.

**Responsibilities**
- Maintain an overview of the existing software development lifecycle (SDLC) procedures within QMENTA.
- Recommend changes or improvements to existing procedures, testing solutions, and technologies that might improve product quality, safety, productivity, and customer satisfaction.
- Estimate, prioritize, plan, and coordinate quality testing efforts included in the SDLC.
- Design and develop the testing plans in a continuous integration/delivery pipeline, including test scripts, results, execution, share responsibilities, deadlines, and test environment.
- Develop test cases based on requirements and implement test plans to assure software meets specifications and design, and supervise inspections.
- Review defects and objective evidence to identify root causes and suggest solutions for improving testing, products, and processes.
- Document test plans prior to releases, test data, and results, and provide the necessary documentation for releases according to our Quality Management System.
- Collaborate with the Chief Product Officer (CPO) to assist him in the definition of the requirements and specifications.
- Analyze product requirements and specifications, the associated risks and mitigation measures during the software development lifecycle.
- Supervise and assist quality engineers in their day-to-day responsibilities, and mentor junior team members to guide them in best practices and technical skills.
- Act as the main bridge between the QARA (Quality Assurance and Regulatory Affairs) team and Engineering/MIR (Medical Imaging Research) teams for quality-related topics.

**Required skills and experience**:

- 5+ years of professional experience as a Quality Assurance Engineer, ideally in medical software.
- Experience in Cloud environments.
- Excellent verbal and written communication skills in English.
- Independent reasoning and critical thinking skills.
- Independent planning of the various parts of a software development lifecycle, acceptance testing, and validating changes for releases
- Meticulous attention to detail.
- Detail-oriented problem solver with a passion for quality

**Desired Qualifications (optional)**:

- Experience in the software development life cycle in a regulated environment, ideally in the Healthcare sector (IEC 62304, IEC 82304, ISO 13485:2016, 21 CFR FDA Part 820, and 21 CFR FDA Part 11).
- Experience working in a CI/CD environment (e.g. Jenkins).
- A can-do attitude and passion for web technologies.

**What we offer**:

- **Competitive salary **that reflects the skills and experience
- **Flexible Work Environment **Flexibility of working hours within our hybrid model
- **Inclusive and multicultural team** Join a vibrant team that celebrates diversity, bringing together over 15 nationalities
- **Health insurance coverage and flexible remuneration package**:

- **Weekly delicious breakfast and teambuildings**:

- **Be a part of a dynamic and fast-growing organization where your contributions truly matter**

Check our VALUES here

**Only CVs in English will be taken into consideration**

If you want to be part of a positive impact in the biotech industry with an international highly qualified team, QMENTA is your place.

Follow your career aspirations to QMENTA for diverse opportunities with a company that provides the growth and strength to build your future.

QMENTA is an Equal Opportunity Employer, committed to employee diversity.