About this role
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
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