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
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