Technical Writer

USA-Technical Writer II (IT)

Location: Swiftwater, PA- Onsite

Duration: Contract till Mar 2027 with possibility to extend

Shift: 1st, Shift Monday thru Friday- 8 am to 4:30

Note:

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

Job Description:

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

QUALIFICATIONS:

• 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.