Technical Writer
2 weeks ago
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
Document Management
Excellent Communication Skills
Pharmaceutical Industry
Technical Documentation
Lean Manufacturing
Technical Writing
Content Management
Biomedical Engineering
Audits
Instructional Design
Manufacturing
Writing Skills
Six Sigma
Able To Work Independently
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