Term of Contract:
• Full time(40 hours/week)
• 12 month duration
The Technical Writer is responsible for supporting the overall GMP upstream and downstream manufacturing process, through the application of broad technical writing experiences, developing standard operating procedures for manufacturing processes as well as routine tasks in the production of bulk biologics therapies.
Requirements:
• Previous experience in Biotechnology/Pharmaceutical Manufacturing
• Excellent written and verbal communication skills
• Proficiency in MS Office, specifically MS Word and Visio
• Strong attention to detail
• Able to write in explanatory and procedural styles for multiple audiences
• Skilled at prioritization and multi-tasking
• Proven experience working in a technical writing position preferred
• Experience with PAS-X/electronic batch records and change management preferred
Education:
• BA preferred
• Science degree (chemistry, biology, engineering, pharmacy) or experience in Life
Sciences technical writing preferred.