OrciMed Life Sciences is a leading pharmaceutical and life sciences company specializing in research, regulatory documentation, and quality compliance. We are committed to innovation and excellence, offering a dynamic work environment for professionals passionate about scientific documentation and SOP management.
Join our team and contribute to high-impact projects in a collaborative, growth-driven workplace!
Job Description: Document Specialist
Key Responsibilities:
✔ Format and manage SOPs (Standard Operating Procedures) ensuring compliance with industry standards.
✔ Apply MS Word guidelines for documentation, including:
- Headers, footers, and version control
- Page setup, styles, and formatting consistency
- Headings & Table of Contents (TOC) generation
✔ Develop, edit, and maintain company documents (SOPs, forms, reports).
✔ Ensure document control and version tracking for regulatory compliance.
✔ Collaborate with cross-functional teams to improve documentation workflows.
Eligibility Criteria:
✅ 1-3 years of experience in scientific documentation (pharma/life sciences preferred).
✅ Strong expertise in MS Word (Styles, Headers, TOC, Version Control).
✅ Knowledge of Good Documentation Practices (GDP) is a plus.
✅ Bachelor’s degree in Life Sciences, Pharmacy, or related fields.
✅ Attention to detail and strong organizational skills.
Benefits & Perks:
💰 Competitive salary package
📈 Career growth opportunities in pharma documentation & compliance
🏢 Flexible & supportive work environment
🌍 Work with industry experts in regulatory and scientific documentation
How to Apply?
📩 Send your resume to: careers@orcimedlifesciences.com
📌 Subject Line: “Application for Document Specialist – [Your Nam
