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