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Technical Writer II

Integrated Resources, Inc

Swiftwater, PA

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JOB DETAILS
SALARY
$45–$50 Per Hour
SKILLS
Biotech and Pharmaceutical, Communication Skills, Current Good Manufacturing Practice (cGMP), Editing, GMP (Good Manufacturing Practices), High Tech Industry, Information Technology & Information Systems, Interpersonal Skills, Laboratory Information Management System (LIMS), Labware, Maintain Compliance, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Microsoft Visio, Microsoft Word, Pharmaceutical Analysis, Presentation/Verbal Skills, Project Tracking, Quality Control, Regulatory Compliance, Regulatory Requirements, Safety Compliance, Safety Training, Standard Operating Procedures (SOP), Team Player, Technical Writing, Time Management, Validation Plan, Writing Skills
LOCATION
Swiftwater, PA
POSTED
13 days ago
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., LabVantage, iLMS, Sequel, or related systems)
  • Experience deploying digital systems (e.g., LabWare, 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.

About the Company

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Integrated Resources, Inc