GMP Technical Writer for Digital Platform Training

Stark Pharma Solutions Inc; Swiftwater (Monroe County); On-site; USD 60,000 - 85,000; Full time

Job summary

Stark Pharma Solutions Inc is looking for a Technical Writer to support the development of user-friendly training materials and documentation in Swiftwater, PA. You will be responsible for creating and maintaining compliant documentation and training content in a GMP-regulated environment.

The ideal candidate will have at least 2 years of experience in technical writing within the pharmaceutical or biotech sectors, ensuring all documentation meets regulatory quality standards.

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.

Responsibilities

• Develop, revise, and maintain technical documentation, training materials, and process-related content.
• Convert technical and operational information into engaging training presentations and user guides.
• Review and update quality documents including SOPs and Work Instructions.
• Ensure all documentation complies with GMP, regulatory, and internal quality requirements.
• Collaborate with cross-functional teams to gather information.
• Assist with document control activities and quality documentation updates.

Skills

Technical Writing

Document Management

GMP Compliance

Cross-Functional Collaboration

Education

Bachelor's degree

Master's or PhD

Tools

Microsoft Word

PowerPoint

Visio

Excel

Outlook

Veeva

LIMS

LabWare

Job description

Stark Pharma Solutions Inc is looking for a Technical Writer to support the development of user-friendly training materials and documentation in Swiftwater, PA. You will be responsible for creating and maintaining compliant documentation and training content in a GMP-regulated environment.

The ideal candidate will have at least 2 years of experience in technical writing within the pharmaceutical or biotech sectors, ensuring all documentation meets regulatory quality standards.