Responsible for designing, developing, and updatingrequired 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 writing and reviewing documents following current Good Documentation Practices (cGMP).
- 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.
Experience: 3 to 6 years
Bachelor's Degree in Science, Engineering, or another technical field.