Associate - Scientific Writing

2 days ago

Bengaluru Karnataka, India Indegene Full time

**Date**:14 May 2025

**Location**:Bangalore, KA, IN
- Looking to jump-start your career?
- We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth.

We are purpose-driven.**We enable healthcare organizations be future ready and our customer obsession is our driving force**.** We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.
- MPharm/Pharm D/ BDS/MDS/PHD (lifeSciences)/ any Life Science Post graduates
- Minimum 2 to 4 years of experience in pharmaceutical companies in regulatory affairs with clinical and regulatory documents Quality Check (QC)
- Responsible for QC review of the document; Perform source data verification, review content for scientific and data accuracy, consistency, basic editorial/formatting aspects (sentence structure, spellings, grammar, format, abbreviations, compliance to style guide, indexing and hyperlinking) and validate if all QC comments/suggestions are incorporated.
- Responsible to ensure that the team strictly adhere to quality standards, confidentiality and security policies of Indegene
- Well-versed in client communication, Interface with clients on a regular basis to meet their expectations

**EQUAL OPPORTUNITY**
- We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

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