Lilly -Analyst – GRA Job in Bangalore

Join the team at Lilly, a global healthcare leader dedicated to improving lives worldwide. We are currently looking for a highly motivated Analyst – GRA to join our team in Bangalore, Karnataka, India. At Lilly, we combine compassion with discovery to develop life-changing medicines, enhance disease understanding, and contribute to our communities through philanthropy and volunteerism. If you are passionate about making a positive impact on global healthcare, we want to hear from you.

Vacancies List:

• Company Name: Lilly
• Location: Bangalore, Karnataka, India
• Category: Research & Development
• Job Type: Full Time Regular
• Job Id: R-54056

Position Title:

Analyst – GRA

Role Category: Research & Development

Department: Chemistry, Manufacturing, and Control (CMC) Editors and Finalizers

Industry Type: Pharmaceutical

Employment Type: Full Time Regular

Job Description:

The Chemistry, Manufacturing, and Control (CMC) Editors and Finalizers play a vital role in converting complex scientific content into error-free, publication-ready documents that meet international standards. This role involves ensuring the accuracy and quality of CMC documents related to regulatory submissions. Key responsibilities include:

Primary Responsibilities:

1. Correcting errors in grammar, style, and syntax.
2. Ensuring data and content accuracy through cross-checking with source documents.
3. Identifying and rectifying flaws in logic and flow.
4. Following style guides/templates provided by the team.
5. Adhering to best practices based on Lilly internal standards.
6. Performing document management services, including launching shells, managing metadata, creating document libraries, and more.
7. Formatting documents to meet Lilly standards.
8. Collecting necessary forms and maintaining documentation.
9. Reviewing and formatting Word files, rendering them into PDFs, and editing PDFs to meet regulatory requirements.
10. Producing final eCTD-compliant PDFs of CMC regulatory documents using publishing software.

Minimum Qualification Requirements:

• M. Pharm or equivalent degree in a scientific or related field.
• Minimum 1 to 2 years of Document Finalization/Document Editing experience for CMC documents and knowledge of maintaining databases.
• RIM knowledge will be preferred.

Additional Preferences:

• Excellent MS Word and Adobe PDF skills.
• Demonstrated teamwork skills and effectiveness.
• Experience in the pharmaceutical industry preferred.
• High attention to detail and superior English-language skills.
• Basic knowledge of CMC (preferred).
• Literature reviewing and evaluation capabilities.
• Ability to multi-task and work under tight timelines.
• Proficiency with Microsoft Word, PowerPoint, Excel, desktop publishing software.