About the Role:

• We are seeking a detail-oriented and experienced Technical Writer with 2–3+ years of experience to join our team.
• The ideal candidate will have a strong command of Word programs, Smartsheet, and familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices). Prior experience in the pharmaceutical or biotech industry—especially in pharma manufacturing is highly desirable.
• This is a hybrid role, requiring 2–3 day onsite per week.

Pay Range: $34 - $37 an hr.

Key Responsibilities:

• Create, write, edit, and format various technical and procedural documents, including:

  • Standard Operating Procedures (SOPs)

  • Business Practices

  • Forms and checklists

  • Technical manuals

  • Installation guides

  • User manuals

• Ensure documentation complies with established format, content, and style guidelines.

• Manage documentation lifecycle through the established Document Processing Review process.

• Distribute and communicate documentation through appropriate media channels, including CDs, intranet, and online training platforms.

• Maintain accuracy, consistency, and high quality across all documentation.

Qualifications:

• Doctorate degree OR

• Master’s degree and 2 years of relevant experience OR

• Bachelor’s degree and 4 years of relevant experience OR

• Associate’s degree and 8 years of relevant experience OR

• High school diploma/GED and 10 years of relevant experience

Required Skill & Experience:

• Experience using Smartsheet

• Proven background in technical writing within a regulated environment

• Knowledge of GMP and GDP compliance

• Experience with document version control systems

• Excellent written and verbal communication skills

• High attention to detail and ability to work independently

Preferred Industry Background:

• Pharmaceutical or biotechnology industry

• Experience in pharmaceutical manufacturing environments is a plus