Technical Writer

  •  

Swiftwater, PA

Industry: Pharmaceuticals & Biotech

  •  

Less than 5 years

Posted 13 days ago

  by    Jitendra Kushwah

Description

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.

 

Skills:

  •         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

 

Education:

 

Bachelor's Degree in Science, Engineering, or another technical field.

$80K - $90K