Technical Writer

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