We are looking for a motivated Front-End Development Intern to join our team. As an intern, you will gain hands-on experience in designing and developing responsive, user-friendly web interfaces using HTML, CSS, and JavaScript. You will collaborate with experienced developers and designers to create engaging web experiences. This is an excellent opportunity to enhance your front-end development skills, work on real-world projects, and contribute to the success of our organization. Key Responsibilities: Develop and maintain web pages using HTML, CSS, and JavaScript. Collaborate with designers to translate mockups and wireframes into functional web interfaces. Ensure websites are responsive and optimized for various devices and browsers. Write clean, efficient, and reusable code following best practices. Assist in debugging and troubleshooting front-end issues. Participate in code reviews and provide feedback to peers. Contribute to improving website performance and user experience. Stay updated with the latest trends and technologies in front-end development. Required Skills: Proficiency in HTML5, CSS3, and JavaScript. Basic understanding of responsive design principles and frameworks like Bootstrap or Tailwind CSS. Familiarity with version control systems like Git. Strong attention to detail and problem-solving skills. Ability to work collaboratively in a team environment. Eagerness to learn and adapt to new technologies. Preferred Skills: Knowledge of front-end frameworks/libraries like React.js , Vue.js , or Angular. Experience with SASS/SCSS or other CSS preprocessors. Familiarity with browser developer tools for debugging. Understanding of accessibility standards (e.g., WCAG). Basic knowledge of backend technologies (e.g., Node.js, APIs) is a plus but not required.

Conduct thorough proofreading and quality checks of medical documents as per FDA and EMA regulatory standards. Accurately interpret scientific terminology and ensure consistency across content. Logically connect and verify scientific data and terms for coherence and correctness. Collaborate with scientists and content experts to resolve QC markups and content discrepancies. Ensure documents are error-free and meet regulatory requirements before submission or publication. Preferred candidate profile Bachelors degree in Science (B.Sc. or B.Pharm). 23 years of relevant experience, preferably with a background in pharmaceutical regulatory labeling. Strong proofreading skills with attention to detail. Excellent analytical skills to identify content gaps, root causes of issues, and suggest practical solutions. Effective verbal and written communication skills, with the ability to interact professionally with internal teams and external clients. Proficient in Microsoft Word, especially in using Track Changes for document review and collaboration.