Technical Writer – Pharma / GMP Environment

Job Title: Technical Writer – Pharma / GMP Environment

Location: Swiftwater, PA (Fully Onsite)
 

Job Description:

We are actively seeking an experienced Technical Writer for a long-term onsite contract opportunity with one of our pharmaceutical clients in Swiftwater, PA.

The selected candidate will work closely with cross-functional teams on a new digital system implementation project focused on converting operational and scientific information into structured training materials and technical documentation.

Key Responsibilities:
• Design, develop, review, and update technical documentation and training materials
• Assist in editing quality documents including SOPs, guidelines, validation master plans, and related documentation
• Ensure all documentation complies with GMP and regulatory requirements
• Create engaging PowerPoint training materials, slides, graphics, and presentations
• Collaborate with business and technical teams to gather and organize information
• Support digital system deployment and documentation activities

Required Qualifications:
• Bachelor’s degree required (Master’s or PhD candidates welcome)
• Minimum 2+ years of experience as a Technical Writer
• Experience working with quality applications such as Veeva, LIMS, LabWare, etc.
• Strong experience with MS Office Suite (Word, Excel, PowerPoint, Visio, Outlook)
• Prior experience in GMP pharmaceutical, biotech, analytical, or manufacturing environments
• Excellent written and verbal communication skills
• Strong interpersonal and team collaboration skills
• Ability to create professional training materials and presentations

Preferred Qualifications:
• Background in Digital IT or Scientific domains
• Experience with QC (Quality Control) activities
• Experience deploying digital systems
• Knowledge of validation processes and compliance documentation