Top 21 Technical writer Jobs in Maryville, Tn

Validation Writer
Tjoapack —Clinton, TN
- Full-time
- Background check
- Microsoft Excel
- Engineering
Quick Apply
Cybersecurity Technical Writer - AI Trainer
DataAnnotation —Tennessee
- $50 - $100 an hour
- Part-time
- Remote
- English
- Mid-level
- Bachelor's degree
- Flexible schedule
Quick Apply
Technical Writer
Management Solutions LLC —Knoxville, TN
- Full-time
- English
- Mid-level
- Office
Procedure Writer
Edgewater Technical Associates —Oak Ridge, TN
- 18 years or older
- Bachelor of Science
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Technical Procedure Writer (3889)
Navarro Inc. —Oak Ridge, TN
- Full-time
- Microsoft Word
- Engineering
- Mid-level
- AD&D insurance
- Paid holidays
Quick Apply
Procedure Writer (Chemical Process) - Hybrid/Remote
Edgewater Technical Associates —Oak Ridge, TN
- Remote
- 5 years
- Engineering
- Senior level
- Disability insurance
- Health insurance
Quick Apply
Technical Writer - Environmental Health and Safety - UTK
University of Tennessee Health Science Center —Knoxville, TN
- $60,000 - $65,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- OSHA
- Mid-level
CCS Service Engineer
Siemens Healthineers —Knoxville, TN
- $89,220 - $122,672 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Disability insurance
- Health insurance
Quick Apply
5d
Senior PR Technical Writer
Ripley PR —Maryville, TN
- 7 years
- Office
- In-person
- Health insurance
- Dental insurance
11d
Technical Procedure Writer
GEM Technologies, Inc. —Oak Ridge, TN
- Full-time
- 18 years or older
- Bachelor's degree
- Senior level
- Health savings account
- Paid holidays
Quick Apply
Technical Procedure Writer, Level V
Akima, LLC —Oak Ridge, TN
- 18 years or older
- Bachelor of Science
- Pass drug screening
Technical Procedure Writer, Level IV
Akima, LLC —Oak Ridge, TN
- 18 years or older
- Bachelor of Science
- Pass drug screening
Procedure Writers
Boston Government Services, LLC —Oak Ridge, TN
- Full-time
- 18 years or older
- Bachelor of Science
- Pass drug screening
- Disability insurance
- Health insurance
Technical Procedure Writer, Level III
Akima, LLC —Oak Ridge, TN
- 18 years or older
- Bachelor of Science
- Pass drug screening
Technical Writer - Environmental Health and Safety - UTK
University of Tennessee - Knoxville —Knoxville, TN
- $60,000 - $65,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Mid-level
- Master's degree
Procedure Writer
Napakiak Ventures —Oak Ridge, TN
- Bachelor of Science
- Bachelor's degree
- Quality control
Quick Apply
Service Writer
Mazzella Companies —Knoxville, TN
- Full-time
- Spanish
- Military
- Computer literacy
- Disability insurance
- Health insurance
Service Writer
Mazzella —Knoxville, TN
- Full-time
- Spanish
- Military
- Computer literacy
- Disability insurance
- Health insurance
Quick Apply

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technical writer jobs near maryville, tn

Validation Writer

Tjoapack -
Clinton, TN

Quick Apply

Job Details

Full-time

Qualifications

GMP
Manufacturing facility experience
Pharmaceutical company experience
Pharmaceutical manufacturing facility experience

Full Job Description

Validation Writer

Clinton, TN | Full-time | Onsite
Department: Technical Services

About Tjoapack

Tjoapack is a global contract packaging organization (CPO) specializing in primary and secondary pharmaceutical packaging and supply chain management services. With more than 30 years of experience, we process millions of medicine packages every year for customers in over 45 countries worldwide.

Operating in Clinton, TN since 2021, Tjoapack is focused on delivering safe, compliant, and reliable packaging solutions—always with the patient at the center of our supply chain.

The Role

As a Validation Writer, you are a key member of the Technical Services team, responsible for developing FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical packaging operations as an entry level technical writer.

Your primary responsibility is entry level Technical Writing- authoring product-specific Master Batch Records (MBRs) executed during production, as well as equipment and component specific validation tests. You will also assist with the execution of qualification activities as needed, supporting new product introductions and validated packaging operations.

This role requires a strong understanding of packaging equipment and processes, along with the ability to clearly communicate technical concepts to diverse internal and external stakeholders.

One year of prior experience in a Pharmaceutical cGMP environment is required for consideration.

What You’ll Do

Process & Equipment Validation

Develop, author, and support execution of validation protocols including FAT, SAT, Engineering Studies (ES), IQ, OQ, and PQ.
Design equipment- and component-specific validation tests.
Assist with the execution of qualification activities as required.
Support Operational and Performance Qualifications for new products introduced to the facility.
Ensure equipment and processes meet GMP, FDA, and customer requirements.

Technical Documentation Development

Create and maintain product-specific Master Batch Records (MBRs).
Develop Master Setup Sheets and Work Instructions supporting validated processes.
Prepare Label Requests and ensure labeling accuracy and traceability.
Ensure documentation supports efficient, compliant, and validated production.
️ Packaging & Component Evaluation

Perform technical evaluations of packaging components and processes.
Assess and document the impact of changes to packaging and serialization processes as they relate to validation and documentation requirements.

Project Support & Collaboration

Participate in cross-functional projects related to product introductions, validation, and process changes.
Collaborate with Engineering, Quality, Operations, and Production teams.
Support training of teams on new documentation, processes, or technologies as needed.

Continuous Improvement

Identify inefficiencies in validation or documentation processes.
Propose and implement process improvements.
Support or initiate RCAs, Change Controls, CAPAs, Risk Assessments, and Validation activities in accordance with Tjoapack procedures.

What We’re Looking For

One year of prior experience in a Pharmaceutical cGMP environment is required for consideration.
Experience in technical and/or validation writing.
Strong attention to detail and ability to follow regulatory requirements.
Excellent verbal and written communication skills.
Proficiency with Office 365 (Word, Excel) and Microsoft Teams.
Familiarity with manufacturing operations and production support.
Ability to manage multiple priorities and meet timelines in a regulated environment.

Why Join Us?

Play a critical role in supporting compliant, validated packaging operations.
Work cross-functionally with Engineering, Quality, and Production teams.
Gain exposure to new product introductions and pharmaceutical packaging validation.
Be part of a growing global organization with long-term stability.
Competitive compensation and benefits with opportunities for growth.

Pre-Employment Requirements ️

All employment at Tjoapack is contingent upon successful completion of:

Background check
Drug screening
Physical examination

Apply Now

If you enjoy technical writing, validation work, and supporting regulated manufacturing environments, we’d love to hear from you.

#TJO123

Quick Apply

Refine Your Search

technical writer jobs in maryville, tn

Validation Writer

Cybersecurity Technical Writer - AI Trainer

Technical Writer

Procedure Writer

Technical Procedure Writer (3889)

Procedure Writer (Chemical Process) - Hybrid/Remote

Technical Writer - Environmental Health and Safety - UTK

CCS Service Engineer

Senior PR Technical Writer

Technical Procedure Writer

Technical Procedure Writer, Level V

Technical Procedure Writer, Level IV

Procedure Writers

Technical Procedure Writer, Level III