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