4 Agile (Scrum) Jobs

Key Deliverables: Create and execute IQ, OQ protocols ensuring GxP compliance Conduct manual and automated testing for functional and performance assurance Maintain validation documentation aligned with regulatory standards Collaborate on continuous improvement and automation initiatives Role Responsibilities: Validate integrated case management systems per SDLC and regulatory needs Report and manage defects with development and quality teams Identify tools to improve test automation and validation workflows Ensure traceability and compliance through structured change control

What will you do Analyze requirements, develop concepts and implement modern Single Page Applications along the entire development lifecycle Implement complex workflows and data handling in applications Write scalable, maintainable and readable code Ensure quality in every aspect of your work, from writing and maintaining documentation, doing code reviews and various levels of testing (UI unit tests, SPA tests, etc.) Collaborate with other teams in an international environment Ensure full security and data privacy compliance of the implementation What will you bring along Motivation to build products that delight our customers A mindset of continuous learning, willingness to share knowledge and learn from others Ability to innovate and find solutions to complex problems A perfect balance between being a strong individual contributor and an empathic team player Ability to communicate effectively with different stakeholders in the company What do you need to have Expertise in programming with languages like Javascript / Typescript and modern web application frameworks like React (preferable), Ember, Angular 2, etc. and adept at HTML, CSS Expert knowledge of key UI design principles Hands-on experience with libraries like jquery & LESS, and Ajax Experience in agile software development (Scrum); Experience in working in scaled agile environments (i.e. multiple agile teams working on one product / platform) is a plus Basic understanding of CI/CD workflow and tools (Gitlab CI/Jenkins/Jenkins-x/...) Knowledge of Java or Python is a plus Bachelor's and/or Master's degree in Computer Science or related field

Key Responsibilities: Deliver high-quality, scalable, and maintainable code independently and with the team. Lead the development team technically, ensure best practices (Agile, TDD, CI/CD) are followed. Actively contribute to planning, stand-ups, sprint reviews, retrospectives, demos, and release planning. Participate in and lead code reviews, performance optimizations, and defect prevention strategies. Collaborate with onsite/offshore teams to clarify requirements and remove blockers. Drive agile delivery of MVPs and ensure timely release with quality metrics like defect density and leakage. Maintain project visibility, team accountability, and agile discipline. Technical Skills: Frontend: Angular 15+, TypeScript, HTML5, CSS3, Jest. Backend: .NET Core, C#, REST APIs, LINQ, Entity Framework, XUnit. Database: MS SQL Server performance tuning and troubleshooting. Tools & Platforms: Git (PRs, commits, merges), CI/CD pipelines, SonarQube, Docker (basic), Messaging systems, Reverse Proxy. Architecture & Patterns: CQRS, Mediator, Repository, JWT & Basic Authentication. Methodologies: Agile (Scrum), TDD, UML. Preferred Experience: Web and mobile app deployment/maintenance experience. Experience in healthcare or life sciences domain. Exposure to SaaS-based applications and cloud delivery models. Comfort in collaborating with European teams. Qualifications : BE in Computer Science, MCA, or equivalent degree with relevant experience.

Let's do this. Let's change the world. We are seeking an experienced Validation Engineer to work on a GxP platform supporting the Regulatory Submission system and Clinical Trial Registry system. This role will be pivotal in ensuring compliance, efficiency, and innovation in the management of data validation processes. The successful candidate will work on a small team and support continuous improvements and automation within the program. This position combines technical expertise, validation experience, and a strong understanding of regulatory requirements. The role also leverages domain and business process expertise to drive ongoing improvements to validation and meets our regulatory and validation procedures. This role involves working closely with developers and business analysts to ensure that the technical requirements for upcoming development are thoroughly elaborated and validated. Roles & Responsibilities: Develop comprehensive test plans and strategies based on project specifications and requirements. Perform manual and automated testing of software applications, including functional, regression, and performance testing. Document and report defects identified during testing and collaborate with development teams for resolution. Maintain detailed records of test plans, test cases, and test results to ensure traceability and compliance. Validate test scenarios against feature acceptance criteria and customer expectations. Ensure system compliance with regulatory requirements for data integrity, traceability, and reliability. Identify opportunities to enhance testing efficiency and minimize manual efforts. Evaluate and adopt tools and technologies to improve automation capabilities. Keep validation documentation updated and aligned with GxP standards. Ensure strict adherence to change management processes for validated systems. Stay informed on industry trends, emerging technologies, and regulatory updates relevant to GxP. Provide expert technical support in validation to optimize quality, efficiency, and cost for developing, troubleshooting, and improving new and existing applications and platforms. What we expect of you: We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Master's degree and 1 to 3 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Bachelor's degree and 3 to 5 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Diploma and 7 to 9 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Experienced in GxP validation process Have 4-5 years of experience in the Pharmaceutical Industry Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technology Experience with Agile software development methodologies (Scrum) Excellent communication skills and the ability to interface with senior leadership with confidence and clarity Experience in writing requirements for the development of a modern web application Strong understanding of GAMP 5 guidelines, 21 CFR Part 11, and Annex 11 Proficiency in automation tools, data systems, and validation software Preferred Qualifications: Experience in Clinical Trial Registry and Regulatory submission publishing systems and processes Knowledge of the Disclose application from Citeline and docuBridge from Lorenz Demonstrated expertise in a scientific domain area and related technology needs Understanding of scientific software systems strategy, governance, and infrastructure Familiarity with low-code, no-code test automation software Technical thought leadership Able to communicate technical or complex subject matters in business terms Knowledge of DevOps, Continuous Integration, and Continuous Delivery methodology Professional Certifications: SAFe for Teams certification (preferred) Soft Skills: Able to work under minimal supervision Skilled in providing oversight and mentoring team members. Demonstrated ability in effectively delegating work Excellent analytical and gap/fit assessment skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Strong presentation and public speaking skills