Responsible for designing, developing, and updating required technical documents associated with improvement projects for Biologics Manufacturing.
Responsible for technical writing/editing for all types of documentation produced within a GMP manufacturing environment.
Experience: 3 to 6 years
Experience writing and reviewing documents following current Good Documentation Practices.
Experience working in a cGMP environment required; biologics or pharmaceuticals preferred.
Ability to interface between operations and support functions and is expected to work effectively with partner functions such as Quality and Manufacturing Technology.
Must be proficient in use of Microsoft Outlook, Word, and Excel.
Bachelor's Degree in Science, Engineering, or another technical field.
Source: Job Diva – Job Listing