What are the responsibilities and job description for the Writer position at Tucker Parker Smith Group (TPS Group)?
Technical Documentation Writer
Location: Brentwood, MO
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Work Arrangement: 100% Onsite
Duration: 6-Month Contract with High Likelihood of Extension/Conversion
Max Pay Rate: $28/hour
About the Role
We are seeking a detail-oriented Technical Documentation Writer to support ongoing documentation initiatives within a regulated pharmaceutical manufacturing environment. This is a traditional technical writing role focused on completing and improving controlled GMP documentation to ensure clarity, compliance, and operational efficiency.
This position offers strong potential for full-time conversion and is ideal for candidates looking to build long-term stability within a growing pharmaceutical organization.
Key Responsibilities
- Author, revise, and finalize Standard Operating Procedures (SOPs), batch records, forms, and related GMP documentation.
- Ensure documents meet regulatory standards and align with internal quality systems.
- Collaborate with Manufacturing, Quality, and Compliance teams to gather technical information and translate it into clear, user-friendly documentation.
- Review existing procedures for accuracy, consistency, and compliance with current GMP requirements.
- Support documentation projects to ensure timely completion of deliverables.
- Maintain document control standards and support continuous improvement of documentation practices.
- Utilize electronic quality systems (including TrackWise, if applicable) to manage document workflows and change controls.
Required Qualifications
- Pharmaceutical GMP experience is REQUIRED.
- 1–3 years of technical writing experience in a regulated pharmaceutical or life sciences environment.
- Strong understanding of Good Manufacturing Practices (GMP) and quality documentation standards.
- Proven ability to write clear, structured, and compliant procedural documentation.
- Proficiency in Microsoft Office (especially Word) with experience formatting controlled templates.
- Strong organizational skills and ability to manage multiple documentation assignments simultaneously.
- Excellent written and verbal communication skills.
Preferred Qualifications
- Experience working with TrackWise quality management system (strong plus).
- Experience supporting manufacturing or aseptic operations documentation.
Salary : $28