Specialist Technical Writing

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:

• Develops, writes, edits, and formats materials such as Standard Operating Procedures, Business Practices, forms, checklists, guide, and related technical and business process documentation.
• When creating, updating and enhancing the documentation, adhere to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality.
• Additionally, this position will be required to administer the processing of documents via the established Document Processing Review process.
• May require communication through a variety of media (e.g., CD, intranet, on-line training, etc.);

Qualifications:

• Bachelor’s degree and 5 years of experience
• Previous experience working in Quality Systems, creating SOP or WI, work independently
• MS Office expertise 
• Previous technical writing experience
• Regulated environment experience
• Document version control experience