_Bring your creative and analytical skills to a team where you'll be inspired, empowered, and rewarded for life by creating products that impact hundreds of thousands of families every day._**Location/Division Specific Information**Mexico/ Software Division**How will you make an impact?**This position is responsible for ensuring that the software development process is compliant with applicable standards, regulations and guidance documents for medical devices**What will you do?**- Lead creation of necessary documentation to comply with regulatory requirements and industry best practices.- Review requirements, specifications, product design documents, validation protocols, test plans, test cases, and other documentation as required and provide timely feedback.- Applies a good working knowledge of Software Development Life Cycle, Design Controls, and other regulatory requirements and agencies as it relates to Design Quality Assurance activities in software development.**How will you get here?****_Education_**Typically requires a Bachelor's degree in an engineering/scientific/Computer systems or quality management or, and a minimum of 3 years related experience**_Experience_**- Understanding of QMS or best engineering practices in Software and Testing- Medical Device industry experience is a plus- Experience with a Risk assessment, Risk-based design- Test automation experience- Agile and scrum hands-on experience**_Knowledge, Skills, Abilities_**- Learning agility- Ownership of your work- Collaboration/relationship building- Effective verbal and written communication skills- Experience with Agile Software Development principles preferred.- Ability to prioritize and manage key deliverables in a dynamic, fast-paced high energy environment. Must be able to handle multiple responsibilities concurrently.- Strong analytical and problem-solving skills.Tipo de puesto: Tiempo completoSalario: $50,000.00 - $75,000.00 al mesTipo de jornada:- Lunes a viernesIdioma:- Inglés (Obligatorio)