Seeking a highly motivated individual to draft, edit and review scientific and technical documents in compliance with quality management systems and regulatory guidelines (GLP / GCLP). The candidate will work closely with scientists and technical staff to support generation of standard operating procedures, method validation reports and nonclinical and clinical study reports. Specific duties will include technical writing, data compilation, table generation and review of reports for quality and consistency.
Excellent technical writing skills with high attention to detail
Ability to work collaboratively in a team environment and communicate effectively
Proficiency in Microsoft Word and Excel
Experience working in a GLP/GCLP regulated setting
Experience with controlled documentation
Candidates with laboratory and/or scientific experience
Working knowledge of Watson LIMS
Candidate must hold a bachelor's degree from an accredited college or university in one of the chemical, physical or biological sciences with at least 3 years of technical writing experience. Candidates with laboratory experience preferred.
Source: Job Diva – Job Listing