Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Develop, write, and edit manufacturing documentation, including SOPs, work instructions, batch records, and technical reports.
- Collaborate with subject matter experts(SMEs) to gather and validate technical information.
- Ensure consistency, clarity, and accuracy of documents to align with regulatory and company standards.
- Monitor and document deviations and Corrective and Preventive Actions (CAPAs) to ensure compliance and continuous improvement.
- Maintain and update existing documentation as processes evolve and improve.
- Conduct document reviews and audits to identify gaps and areas for improvement.
- Support regulatory and quality audits by providing documentation as needed.
- Utilize document management systems to track changes and approvals efficiently.
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
- Bachelor’s degree in Biomedical Engineering, Life Science, or a related field
- 2+ years of experience in Technical Writing within the pharmaceutical industry
- Strong understanding of cGMP, and global standards.
- Experience with process flow diagrams, technical illustrations, and instructional design
- Familiarity with Lean Manufacturing and Six Sigma principles.
- Knowledge of digital documentation tools and content management systems.
- Strong documentation and technical writing skills.
- Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
- Excellent communication skills, both written and verbal, in English
