**Job Summary** The Reg Affairs-Med Writing role involves supporting regulatory affairs and medical writing tasks within a hybrid work model. The candidate will contribute to research and development processes ensuring compliance with regulatory standards. With a focus on MS Office and MS Excel. **Responsibilities** + Collaborate with cross-functional teams to ensure regulatory compliance in medical writing tasks. + Develop and maintain documentation related to regulatory affairs and research and development processes. + Utilize MS Office and MS Excel to create edit and manage regulatory documents efficiently. + Ensure accuracy and clarity in all written communications and documentation. + Support the preparation and submission of regulatory documents to relevant authorities. + Conduct thorough research to stay updated on regulatory guidelines and industry standards. + Provide insights and recommendations to improve regulatory processes and documentation quality. + Assist in the development of strategies for regulatory submissions and approvals. + Coordinate with stakeholders to gather necessary information for regulatory documentation. + Monitor and track regulatory submissions and approvals to ensure timely completion. + Contribute to the continuous improvement of regulatory business processes and services. + Maintain confidentiality and integrity of sensitive regulatory information. + Communicate effectively with team members and stakeholders to ensure alignment on regulatory requirements. **Qualifications** + Demonstrate proficiency in MS Office and MS Excel for efficient document management. + Possess strong knowledge of regulatory business processes and services. + Exhibit expertise in regulatory affairs ensuring compliance with industry standards. + Show experience in research and development contributing to innovative solutions. + Display excellent communication skills in English both written and spoken. + Have a keen eye for detail and accuracy in documentation. + Demonstrate ability to work collaboratively in a hybrid work model. + Show adaptability to changing regulatory environments and guidelines. + Possess problem-solving skills to address regulatory challenges effectively. **Certifications Required** Certified Regulatory Affairs Professional (RAPS) Microsoft Office Specialist Certification \#LI-CTSAPAC Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.