As a Backend Developer with 2 to 6 years of experience, you will be responsible for designing complex and generic algorithms. Your role will involve working with data structures, REST API, NodeJS, XML, and JSON. It would be beneficial to have knowledge of Python, Angular, or React Framework. Additionally, experience with source code management in Github and proficiency in writing Typescript will be essential for this position.,
As a Full-Stack Developer with 5 to 8 years of experience, you will be responsible for utilizing your expertise in Angular, Bootstrap designs, XML, JSON, NodeJS, and Express to build APIs, including routing, middleware, and libraries. You will have experience in developing a microservices-based architecture and designing complex and generic algorithms. It would be beneficial if you have knowledge of Python, Angular, or React Framework. Your role will also involve creating a Database Access Layer (DAL) with SQL Databases such as Oracle or MySQL. Additionally, experience in creating deployable packages/installers for Windows and Linux platforms is a bonus.,
As a Frontend Developer with 2 to 6 years of experience, you will be responsible for implementing user interfaces using technologies such as Angular, Bootstrap designs, XML, JSON, and source code management in GIT. Your role will involve a deep understanding of Java-script, DOM, HTML5, and Styles like CSS and SCSS. In this position, you will need to have a solid grasp of best practices for consuming REST API, including knowledge of GraphQL. Additionally, you will be expected to apply UI/UX principles based on end-user preferences to create intuitive and user-friendly interfaces.,
SENIOR CONSULTANT: CSV (Experience: 4 to 6 Years in CSV) Roles and responsibilities: Working experience in CSV (Computer System Validation) in Life Sciences domain. Good knowledge of GxP regulations and GAMP 5 Guidelines. Must have experience and knowledge of 21 CFR part 11 and EU Annex 11 regulations. Experience in defining the validation strategy, approach, and alignment with customer on QMS. Good knowledge of good Documentation Practices. Experience in authoring of CSV deliverables such as Validation Plan, Test Plan, RTM, Test Summary and Validation Summary Report, GxP Assessments, 21 CFR Part 11 assessments and System Release Notice. Strong understanding of pharmacovigilance, regulations, guidelines for difference geographic location and Validating Safety Systems. Reviewing & Authoring the CSV deliverables such as IQ, OQ and PQ scripts. Experience of QA in FDA / EMEA regulated environment is preferred.