Technical Writer

4 weeks ago


Frederick, Maryland, United States GForce Life Sciences Full time
Job Title: Technical Writer

The Technical Writer is a crucial member of the GForce Life Sciences team, responsible for creating high-quality documentation that supports the company's GMP upstream and downstream manufacturing process.

Key Responsibilities:

  • Develop and maintain standard operating procedures (SOPs) for manufacturing processes and routine tasks.
  • Generate and revise manufacturing batch records in electronic batch record systems (PAS-X) and document management systems.
  • Collaborate with subject matter experts across multiple departments to review and approve documentation and changes.
  • Manage updates and revisions to technical process documentation.
  • Self-manage time to complete work based on critical timelines.

Requirements:

  • Previous experience in Biotechnology/Pharmaceutical Manufacturing.
  • Excellent written and verbal communication skills.
  • Proficiency in MS Office, specifically MS Word and Visio.
  • Strong attention to detail.
  • Able to write in explanatory and procedural styles for multiple audiences.
  • Skilled at prioritization and multi-tasking.
  • Proven experience working in a technical writing position preferred.
  • Experience with PAS-X/electronic batch records and change management preferred.

Education:

  • BA preferred.
  • Science degree (chemistry, biology, engineering, pharmacy) or experience in Life Sciences technical writing preferred.

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