Medical Writer Jobs at Syngene | MSc Life Science Graduates Apply Now
Syngene International Ltd., a global leader in discovery, development, and manufacturing services, is hiring a skilled Medical Writer in Bangalore. This role offers the opportunity to collaborate with leading pharmaceutical and biotech companies worldwide, producing high-quality clinical and scientific documents for regulatory submissions. Join a team that thrives on innovation and excellence in medical writing.
- Job Position: Medical Writer
- Location: Bangalore, Karnataka, India
About the Company:
Founded in 1993, Syngene International Ltd. is a world-class, innovation-driven organization providing integrated scientific services to industries including pharmaceuticals, biotechnology, nutrition, and specialty chemicals. Partnering with global leaders like Bristol-Myers Squibb, Amgen, GSK, and Merck KGaA, Syngene’s 4,240+ scientists work collaboratively to accelerate research, improve R&D productivity, and reduce the cost of innovation for clients worldwide.
Job Description:
The Medical Writer will independently develop and finalize clinical and scientific documents for regulatory submissions, including bioanalytical reports, Clinical Study Reports (CSRs), and sections of eCTD modules across various therapeutic areas and phases of clinical research. The role involves collaboration with internal and external clients, ensuring compliance with regulatory guidelines, and delivering projects on time with the highest quality standards.
Key Responsibilities:
- Develop and finalize clinical/scientific documents for regulatory submissions.
- Collaborate with internal/external clients for effective communication.
- Manage writing and review processes to ensure timely delivery.
- Ensure compliance with applicable guidelines, SOPs, and style guides.
- Perform documented QC checks on deliverables and address findings.
- Conduct literature searches/reviews for background scientific content.
- Follow the supervisor’s instructions and complete the assigned tasks.
Qualifications:
- Graduate or Master’s degree in Life Sciences.
- 2–4 years of experience in medical writing.
- Strong understanding of clinical research and regulatory guidelines.
- Proficiency in MS Word, PowerPoint, and related tools.
- Strong communication, adaptability, time management, and professionalism.
Benefits of Joining:
- Opportunity to work with leading global pharmaceutical and biotech companies.
- Exposure to diverse therapeutic areas and regulatory frameworks.
- Career growth in a reputed innovation-driven organization.
- Collaborative and inclusive work culture.
- Continuous learning through training programs, including EHS measures.
