Technical Procedure Writer

📋 Description

• Manage controlled document workflows from authoring and review through approval, updates, change
• Support project teams in developing, revising, and maintaining global and local policies
• Coordinate high volumes of document updates across multiple regions, projects, and stakeholders.
• Identify documents requiring updates in response to planned process, regulatory, or operational
• Coordinate editing, review, feedback, and approval activities across geographically distributed
• Support document authors by recommending clear wording, effective presentation, appropriate

🎯 Requirements

• 3+ years of professional experience in technical writing, with a strong focus on SOPs and Work
• 3+ years of experience managing documents throughout the complete documentation lifecycle
• Associate's or Bachelor's degree in a relevant field.
• Strong expertise in SOP writing techniques and the ability to transform complex technical
• Experience working with electronic document management systems; familiarity with Veeva is an
• Advanced proficiency in Microsoft Office applications, particularly Word, PowerPoint, and Excel.

🎁 Benefits

• Remote working opportunity from India.
• Opportunity to work on global quality and compliance projects within the pharmaceutical and life
• Exposure to international teams and documentation processes across multiple regions and time zones.
• Opportunities to strengthen expertise in SOP development, controlled document management, and
• Collaboration with multidisciplinary professionals across quality, pharmacovigilance, technology
• An inclusive and collaborative work environment that values diversity, innovation, and professional