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Technical Writer II

Job in Swiftwater, Monroe County, Pennsylvania, 18370, USA
Listing for: Integrated Resources, Inc
Full Time position
Listed on 2026-06-07
Job specializations:
  • IT/Tech
    Technical Writer, Data Analyst
Salary/Wage Range or Industry Benchmark: 45 - 50 USD Hourly USD 45.00 50.00 HOUR
Job Description & How to Apply Below
Title:
Technical Writer II

Location:

Swiftwater, PA
Duration: 9 Months+ Possible Extension
Pay Range: $45- $50/hr

Manager Notes:
  • Role will work with a team on a new digital system to convert information into training materials.
  • Schedule:
    Monday Friday, 8:00 AM 4:30 PM (slight flexibility)
  • Fully onsite position
Required Experience/Skills:
  • Minimum bachelor s degree required; master s and PhD candidates are welcome
  • Preferred areas of study: IT or sciences Minimum of 2+ years of experience in a similar role; more years of experience is acceptable.
Nice-to-Have / Preferred Skills:
  • Background in digital IT or scientific fields Experience with QC (quality control) activities
  • Experience with LIMS systems (e.g., Lab Vantage, iLMS, Sequel, or related systems)
  • Experience deploying digital systems (e.g., Lab Ware, LIMS) strongly preferred Knowledge of validation processes is a plus
  • Previous experience in pharmaceutical, analytical, or biotech environments (e.g., Veeva) preferred
  • Proficiency in PowerPoint with the ability to create training materials, including slides and graphics Strong presentation skills
Description
  • The OneLIMS EM project technical writer is responsible for supporting on-time implementation of OneLIMS 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.
Key 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.
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