- Develop and maintain standard operating procedures (SOPs) for the RND department.
- Create and update manuals, work instructions, and training materials.
- Ensure that all documentation complies with regulatory requirements and pharmaceutical standards.
- Collaborate with various teams to gather information and update documentation as needed.
- Organize and maintain electronic and physical documentation systems for easy access and retrieval.
- Review and edit documentation for accuracy, consistency, and clarity.
- Assist in training staff on proper documentation procedures and requirements.
- Identify opportunities for continuous improvement in the documentation process.
Qualifications:
- Major in a related field such as pharmaceutical science, life science, or a related discipline to prepare for a successful career in the pharmaceutical industry.
- Basic pharmaceutical manufacturing process and GMP knowledge are required
- Proven experience in a documentation role, preferably in a manufacturing environment.
- Strong writing and editing skills with excellent attention to detail.
- Knowledge of document management systems and tools.
- Ability to work collaboratively with cross-functional teams.
- Familiarity with regulatory requirements and standards applicable to the pharmaceutical industry.
- Strong organizational and time-management skills
