Technical Writer

Stark Pharma Solutions is seeking a Technical Writer for a 6-Month Contract position in Swiftwater, PA, within the Pharmaceutical / Biotech Manufacturing industry.

Position Overview

We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical and quality-related content into user-friendly training materials and documentation. This role will work closely with cross-functional teams to create compliant documentation, training content, and process materials within a GMP-regulated environment.

The ideal candidate will have experience in technical writing, quality systems documentation, and digital system deployments within pharmaceutical, biotechnology, laboratory, or manufacturing environments.

Key Responsibilities

• Develop, revise, and maintain technical documentation, training materials, and process-related content.
• Convert technical and operational information into engaging training presentations, user guides, and instructional materials.
• Review, edit, and update quality documents including:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Guidelines
  • Validation Master Plans
  • Quality System Documentation
• Ensure all documentation complies with GMP, regulatory, and internal quality requirements.
• Collaborate with Quality, IT, Laboratory, and Operations teams to gather information and create accurate documentation.
• Support digital transformation initiatives by developing training materials for new system implementations.
• Assist with document control activities and quality documentation updates.
• Create visual content, process flows, diagrams, and presentations using PowerPoint and Visio.
• Participate in training development and delivery activities as needed.

Required Qualifications

• Bachelor's degree required; advanced degrees (Master's or PhD) are welcome.
• Minimum 2+ years of experience in Technical Writing, Documentation Management, or a related role.
• Experience working within GMP-regulated pharmaceutical, biotech, laboratory, or life sciences environments.

Hands-on Experience With Quality Systems And Applications Such As

Veeva
LIMS
LabWare (preferred)

Proficiency With

Microsoft Word
Excel
PowerPoint
Visio
Outlook

Strong technical writing, editing, and document management skills.

Excellent verbal and written communication abilities.

Strong interpersonal skills with the ability to work effectively in cross-functional teams.