Documentation Specialist

Position title
Documentation Specialist
Description

Previous Pharmaceutical/Biotech/Medical Device experience is mandatory.

Responsibilities
Responsibilities 
  • Will be responsible for updating master batch records and SOP.¬†
  • This person will need to be trained for Change Controls, SAP MERP system, SOP and MBR author.¬†
  • Minimum 5 years' experience in Pharma cGMP environment with Technical Writing and Documentation experience.
 
Qualifications
Technical Requirements
  • Minimum 5 years' experience in Pharma
  • Technical Writing and Documentation experience.
  • Solid grasp of manufacturing process equipment and cGMP
  • Strong attention to detail
  • Ability to organize and prioritize work
  • Proficient with MS Office applications
  • Strong analytical and problem-solving abilities
  • Strong verbal and technical communication skills
Employment Type
Full-time
Duration of employment
12+ Months
Job Location
Lincoln , Nebraska, United States
Date posted
February 16, 2023
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