Technical Writer

Key Responsibilities:

• Draft and maintain technical documents including summary reports, test criteria, and conclusion reports.
  
  
• Support validation activities by compiling data and writing documentation (ability to read protocols required).
  
  
• Follow up on issues through change control and deviation systems.
  
  
• Collaborate with validation, engineering, and QA teams to ensure compliance with AbbVie standards.
  
  
• Maintain version control and documentation in electronic systems.
  
  

Requirements:

• Bachelor's degree in Life Sciences, Engineering, or related field.
  
  
• Minimum 2 years' experience in technical writing, validation, or documentation in pharma/biotech/medical devices.
  
  
• Familiarity with GMP, validation, and change control processes preferred.
  
  
• Strong attention to detail with good written communication skills.
  
  
• Ability to manage multiple tasks under tight timelines.