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
Hiring organization
Employment Type
Full-time
Duration of employment
12+ Months
Job Location
Lincoln , Nebraska, United States
Date posted
February 16, 2023
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