We are looking for a highly skilled and experienced skilled to join our team as Regulatory Affairs - MSTG in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong background in regulatory affairs and experience working with pharmaceutical companies.

Roles and Responsibility
- Develop and implement regulatory strategies to ensure compliance with relevant laws and regulations.
- Prepare and review regulatory documents, including clinical trial applications and marketing authorizations.
- Collaborate with cross-functional teams to ensure timely submission of regulatory documents.
- Monitor and analyze changes in regulatory requirements and develop plans to implement necessary changes.
- Provide training and guidance to internal stakeholders on regulatory requirements and procedures.
- Review and approve regulatory submissions,



such as clinical trial applications and marketing authorizations.

Job Requirements
- Strong knowledge of regulatory requirements and guidelines governing pharmaceutical companies.
- Experience in preparing and reviewing regulatory documents, including clinical trial applications and marketing authorizations.
- Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams.
- Strong analytical and problem-solving skills, with attention to detail and the ability to meet deadlines.
- Ability to work in a fast-paced environment and adapt to changing priorities and deadlines.
- Strong understanding of regulatory software and systems, with the ability to learn new systems quickly.

📌 Regulatory Affairs Professional (Mumbai)
🏢 Naukri Healthcare Jobs
📍 Mumbai