N
Specialist 3, Technical Writing
Net2Source
- 🇺🇸 United States
- Hybrid
- 11 hours ago
- $39.00 – $39.41 / hour
- GMP
- Adobe Acrobat
- Technical Writing
11 hours ago
Who We Are
Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price.
Job Title: Technical Writer
Location: Fort Washington, PA
Contract Duration: 12 months (Possible extension)
Pay Rate: $39.41/hr on W2 (No Benefits)
Job description:
Hours Monday to Friday 8:30am to 5:00pm
We are seeking a detail-oriented Technical Writer to support the development, revision, and management of manufacturing and engineering documentation within a GMP-regulated environment. This role will be responsible for converting complex engineering, validation, and technical documents into clear, compliant, and user-friendly Standard Operating Procedures (SOPs) and other controlled documentation.
The ideal candidate will have experience working in a regulated pharmaceutical, medical device, consumer health, or life sciences environment and possess strong document management skills using MS Word and Adobe Acrobat. This position requires a significant on-site presence initially to build relationships with stakeholders, facilitate document reviews, and drive approvals and signatures through completion.
Key Responsibilities
Review and interpret engineering, technical, validation, and operational documents.
Transform technical content into clear, concise, and compliant SOPs, work instructions, and controlled documents.
Collaborate with engineers, quality, validation, manufacturing, and cross-functional teams to gather and verify technical information.
Ensure documentation aligns with GMP requirements, company standards, and document control procedures.
Manage document review cycles, incorporating stakeholder feedback and maintaining version control.
Coordinate approval workflows and actively facilitate the collection of required signatures and approvals.
Maintain documentation accuracy, consistency, formatting, and traceability.
Utilize MS Word to develop and format professional documentation templates and final deliverables.
Use Adobe Acrobat to review, edit, compile, and manage controlled PDF documentation.
Support document archival, revision management, and document management system activities as required.
Identify opportunities to improve documentation processes and standardization.
Timing and Duration
The Technical Writer is needed to start immediately to become familiar with the site's equipment, systems, processes, and key stakeholders. The anticipated assignment duration is October 1, 2026 through October 1, 2027. Workload demand is expected to be highest during project initiation and throughout Q1 2027, as a significant volume of engineering and operational documentation will require conversion into SOPs and controlled documents. Following this peak period, the workload is expected to gradually decrease, transitioning to a part-time level of support for the remainder of the engagement while document updates, reviews, approvals, and finalization activities are completed.
Required Qualifications
Bachelor's degree in Technical Writing, English, Communications, Engineering, Life Sciences, or a related field, or equivalent experience.
2-4 years of technical writing experience in a GMP-regulated environment.
Experience creating and editing SOPs, work instructions, controlled documents, or quality system documentation.
Proficiency in MS Word, including advanced formatting, styles, templates, tables, and document controls.
Proficiency in Adobe Acrobat for document editing, review, and PDF management.
Strong attention to detail with excellent proofreading and editing capabilities.
Ability to interpret technical and engineering information and translate it into end-user documentation.
Strong organizational, communication, and stakeholder management skills.
Preferred Qualifications
Experience supporting pharmaceutical, consumer health, biotechnology, medical device, or manufacturing operations.
Familiarity with document management systems and controlled document workflows.
Experience working with Quality, Validation, Engineering, or Manufacturing teams.
Knowledge of GMP documentation practices, data integrity principles, and compliance requirements.
Work Arrangement
On-site in Fort Washington, PA during onboarding and initial engagement period to support stakeholder collaboration, document reviews, approvals, and signature collection.
Opportunity for a hybrid schedule (1-2 remote days per week) once the individual has established working relationships, gained familiarity with documentation processes, and can operate independently.
Key Success Factors
Ability to rapidly understand technical and engineering content.
Strong ownership of documentation deliverables from draft through approval.
Excellent collaboration skills and ability to drive documents to completion.
Commitment to quality, compliance, and continuous improvement.
This role is ideal for a technical writer who enjoys partnering closely with engineering and quality teams to ensure critical GMP documentation is accurate, compliant, and ready for execution.
Why Work With Us?
We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.
Our Commitment to Inclusion & Equity
Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.
Awards & Recognition
• America's Most Honored Businesses (Top 10%)
• Fastest-Growing Staffing Firm by Staffing Industry Analysts
• INC 5000 List for Eight Consecutive Years
• Top 100 by Dallas Business Journal
• Spirit of Alliance Award by Agile1
Ready to Level Up Your Career?
Click Apply Now and let's make it happen.
Best regards,
[[YourFirstName]] [[YourLastName]]
[[YourTitle]]
[[YourAddress]]
Specialist 3, Technical Writing · Net2Source