Job Description
Job Summary:
- The One LIMS EM project technical writer is responsible for supporting on-time implementation of One LIMS EM global system for the Swiftwater, PA site.
- The candidate must perform tasks in an efficient, cGMP compliant, and safe manner.
- Success in this position requires the individual to be adaptable and react quickly to changing priorities in a high-stress environment.
- The candidate is required to complete Safety and Compliance training and associated training modules.
Duties and Responsibilities:
- Design, develop, and update required technical documentation.
- Assist with the editing of quality documents (SOP’s, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
- Create Training slides and content.
- Support Future state process mapping.
- Organize, track and plan master data review.
- Track and mange project specific deliverables.
Qualification:
- Bachelor’s Degree required.
- Prior experience with quality applications, such as Veeva, LIMS
- Prior experience with MS Word, Excel, PowerPoint, Visio and Outlook
- Prior work experience in a good manufacturing practices (GMP) environment
- Must possess sound interpersonal and information gathering skills, be able to relate well to others and have the ability to work in a team environment, effectively interacting with others
- Excellent verbal and written communication skills.
- Minimum of 2 + years of related experience.