Agreement Type: 3-6 Month Contract Location: Remote (UAE Hours) Whiteshield is a global advisory firm helping governments navigate big, world-shaping challenges - from economic transformation to education, employment, and innovation. We work at the intersection of policy, data, and technology, building products that don’t just inform decisions, but improve lives. If you’re motivated by impact and purpose - Whiteshield is for you. WHAT YOU’LL OWN •⁠ ⁠Develop, maintain, and execute test cases for functional, regression, integration, UAT, and automation testing. •⁠ ⁠Perform thorough manual and automation testing on web applications covering UI, functional, responsiveness, and end-to-end scenarios. •⁠ ⁠Contribute towards Designing, implementing and maintaining automation scripts for regression and smoke testing using industry-standard tools (e.g., Selenium, Playwright). •⁠ ⁠Document test results, report bugs, and track them to closure using JIRA. •⁠ ⁠Collaborate with product and engineering teams to clarify requirements, identify edge cases, and ensure optimal test coverage. •⁠ ⁠Contribute to test planning, estimation, and execution in alignment with Agile/Scrum workflows. •⁠ ⁠Participate in release validation, post-release testing, and continuous integration pipelines.

Perform verification and validation activities for cloud systems, analyze trends to identify process improvements, and address functionality and performance issues to ensure optimal system configurations.

Role Description As our second QA Engineer, you will take real ownership of quality across our products and help shape how QA is built in our team from the ground up. Working closely with our QA Lead, you will independently drive test planning, build automation, and improve quality standards across the entire development lifecycle — from frontend to cloud infrastructure. You’ll work with cutting-edge technologies including AI-based computer vision, browser-based 3D visualization, and modern cloud systems — all contributing to software that helps clinicians make faster and more accurate diagnoses. Responsibilities - Take ownership of test planning for releases — from defining scope to keeping documentation up to date. - Build and maintain automated tests using Playwright across our frontend and backend systems. - Test and validate our cloud-based infrastructure (AWS), making sure everything runs reliably in production. - Work closely with engineers, product managers, and regulatory stakeholders to ensure smooth and high-quality releases. - Investigate bugs, identify root causes, and help improve overall product stability. - Track and improve quality over time by looking at metrics like bugs per release or test coverage. - Continuously challenge and improve how we approach testing as a team. Qualifications - 3+ years of experience in software quality assurance. - Strong experience with test automation (ideally Playwright). - Solid programming skills (Python and/or TypeScript). - Experience with testing frameworks (e.g. pytest or similar). - Familiarity with CI/CD pipelines, version control, and Docker. - Comfortable working in Linux environments. - Ability to work independently and take ownership of test planning. Nice to have - Experience with AWS or cloud-based systems. - Exposure to medical software or regulated environments (FDA, CE). - Experience with performance or load testing. - Basic understanding of security testing. Benefits - Use your personal benefits budget flexibly and choose the perks that suit you best! - Focus on what matters: competence, personality, and commitment are more important than formalities or the study program you chose. - Your work helps make disease diagnosis faster, more precise, and more manageable. - Join a highly motivated, interdisciplinary team with fast decision-making processes and a collaborative atmosphere. - Work remotely or from our office in Berlin-Kreuzberg - whatever suits you best.

Role Description Join our Pharma Services team and be a part of a leading contract development and manufacturing organization (CDMO) offering end-to-end services for drug development, clinical trial logistics, and commercial manufacturing! Biotech and biopharma companies trust us for our speed, flexibility, and quality across every phase of drug development. With worldwide locations, we support active pharmaceutical ingredients (APIs), biologics, cell therapy, viral vectors, formulation, clinical trials, logistics, commercial manufacturing, and packaging. Help us enable many major therapies on the market today and drive the future of healthcare! How will you make an impact? By executing key deliverables for the implementation of a practical, proactive, sustainable, scalable, and effective Quality Risk Management Program within the Pharma Services Group. Must be highly organized with an ability to multi-task, work and communicate across multiple sites, different business units, and functions, encompassing the full product life cycle, from early product & process development through commercial manufacturing. Will assist in developing and deploying global processes and systems that must effectively work for multiple sites and will ensure and facilitate their adoption while using industry standard methodologies and body of knowledge and incorporating different requirements and expectations from various regulatory bodies. The position will be in the Global Quality Systems – Quality Operations Team and will report to the Director of Quality Risk Management. What You Will Do: - Provide leadership and guidance for installing an effective global Quality Risk Management program. - Implement the Quality Risk Management Program Roadmap and Risk Maturity Model, and support execution of corresponding Gap Assessments. - Work with different support functions business partners to manage key elements (e.g., Leadership, Program + Tools, Training, Culture) contributing to an effective Quality Risk Management installation. - Partner and collaborate with the different Global Quality Systems groups (e.g., Supplier Quality, Digital Quality Systems, Lab Systems & Technology, Quality Operations, Global Compliance, Quality Academy, and Quality Assurance Systems) from a Quality Risk Management standpoint. - Identify, facilitate, and implement continuous improvement projects related to Quality Risk Management processes and systems thru the adoption of Practical Process Improvement (PPI) Business System. - A Quality Risk Management SME. - Serve as a Lead / SME in Quality Risk Management governance processes. - Leverage Quality Risk Management practitioners across the network to support sites in the region. - Ensure risk assessments are conducted at required intervals and frequencies. - Manage the global Risk Register process / program. - Actively contribute in the Community of Practice. - Provide Quality Risk Management training. - Implement 'Pilot' type of initiatives directly or indirectly related to the Quality Risk Management program. Up to 25% travel required. Qualifications - Bachelor's Degree or higher in Chemistry, Biochemistry, Engineering, or other physical science degrees with relevant work experience. Requirements - Minimum of 7 years' experience in pharma/biopharma regulated industry (GxP) with strong direct hands-on pharmaceutical experience in Quality Risk Management processes, QA, Operations, Technical Services, R&D, or a combination, with a minimum of 4 years' validation experience. - Strong project management experience with ability to work in matrix / remote environment. - Proven Project Management experience. - Ability to prioritize multiple tasks across a portfolio of projects. - Ability to drive continuous improvement / operational excellence. - Ability to work independently with little supervision, especially remotely. - Proficiency in Microsoft Office Suite (Teams, Word, Excel, PowerPoint, etc.). - Ability to communicate via web-based conferencing / collaboration platforms. - Strong written and verbal communication skills and effective presentation skills. - Ability to influence peers and Quality Risk Management practitioners to overcome common pitfalls & paradigms (e.g., 'one-off' activity, an additional task, 'gray' area, not adding new value) thru the practical adoption of effective Quality Risk Management. Benefits - Medical, Dental, & Vision benefits-effective Day 1. - Paid Time Off & Designated Paid Holidays. - Retirement Savings Plan. - Tuition Reimbursement.