Top 1096 Procedure Writer Jobs

Validation Writer
Tjoapack —Clinton, TN
- Full-time
- Background check
- Microsoft Excel
- Engineering
Quick Apply
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos - Clinical and Corporate - Prod —New Jersey
- $95,000 - $210,900 a year
- Full-time
- Microsoft Word
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Senior Technical Documentation Writer/Specialist II
ONEIL —Greenville, NC
- $27 - $28 an hour
- Overtime
- Hybrid work
- Research
- Mid-level
- Office
- Dental insurance
- 401(k)
Quick Apply
California Based Federal & State Grant Writer – Municipal Clients (1–3 Years Experience)
Blais & Associates —California
- From $25 an hour
- Part-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Research
- 401(k)
- 401(k) matching
Quick Apply
Technical Writer I
Paragon Force, Inc —Crane, IN
- $22.00 - $26.50 an hour
- Full-time
- Mid-level
- Office
- Microsoft Office
- Health savings account
- Health insurance
Quick Apply
Health Writer & Content Creator
Thrive Global Holdings, Inc. —Remote
- $115,000 - $130,000 a year
- Full-time
- Remote
- Mid-level
- 10 years
- Health insurance
- Dental insurance
Quick Apply
10d
Technical Writer
Software Technology Inc —Remote
- Temporary
- Remote
- Microsoft Word
- English
- Analysis skills
Quick Apply
Technical Writer
Accenture Federal Services —Remote
- $91,300 - $184,500 a year
- Remote
- English
- Research
- Mid-level
Technical Writer - Homeland Security
Team Carney —Remote
- Full-time
- Microsoft Word
- Research
- Mid-level
- Paid parental leave
- Health savings account
Quick Apply
Technical Writer/Editor III
DirectViz Solutions, LLC —Remote
- $80,000 - $90,000 a year
- Full-time
- Remote
- Microsoft Excel
- 5 years
- English
- Health insurance
- Paid time off
Quick Apply
Technical Writer
Fresenius Kabi —Pleasant Prairie, WI
- $70,000 - $80,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Background check
- Bachelor of Science
- Wellness program
- Paid holidays
Quick Apply
10d
Technical Writer
Planned Systems International, Inc. —Remote
- Remote
- Microsoft Outlook
- Customer service
- 5 years
- AD&D insurance
- Disability insurance
Medical Writer
BGBx —Remote
- $70,000 - $95,000 a year
- Full-time
- Remote
- Medicine
- Research
- Mid-level
- Paid holidays
- Health insurance
Quick Apply
10d
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 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 Writer
ERP International —Fort Meade, MD
- $70,000 - $85,000 a year
- Online Application
- Microsoft Word
- English
- Bachelor's degree
- Health insurance
Technical Writer - 508 Documentation Specialist
General Dynamics Information Technology —Remote
- $74,800 - $101,200 a year
- Remote
- Microsoft Word
- Microsoft Excel
- Oracle
- Paid holidays
- 401(k) matching
4d
Regulatory Writing Contractor
Med Communications —Remote
- Contract
- Medicine
- Microsoft Outlook
- 5 years
Quick Apply
Technical Writer
AAC Inc —Vienna, VA
- $75,000 - $88,000 a year
- Bachelor of Science
- English
- Mid-level
Quick Apply
Medical Writing III
Solventum —Remote
- $137,439 - $167,981 a year
- Full-time
- Remote
- 7 years
- Microsoft Excel
- English
- Health savings account
- Disability insurance

I want to receive the latest job alert for Procedure Writer

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Validation Writer

Tjoapack -
Clinton, TN

Quick Apply

Job Details

Full-time

Qualifications

GMP
Manufacturing facility 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 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 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.

Quick Apply

Refine Your Search

Procedure Writer jobs

Validation Writer

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Senior Technical Documentation Writer/Specialist II

California Based Federal & State Grant Writer – Municipal Clients (1–3 Years Experience)

Technical Writer I

Health Writer & Content Creator

Technical Writer

Technical Writer

Technical Writer - Homeland Security

Technical Writer/Editor III

Technical Writer

Technical Writer

Medical Writer

Procedure Writer (Chemical Process) - Hybrid/Remote

Technical Procedure Writer

Technical Writer

Technical Writer - 508 Documentation Specialist

Regulatory Writing Contractor

Technical Writer

Medical Writing III

I want to receive the latest job alert for Procedure Writer

Related Searches

Explore jobs in more locations

About Tjoapack

The Role

What You’ll Do

What We’re Looking For

Why Join Us?

Pre-Employment Requirements ️

Apply Now

Job Seeker Tools

Employer Tools

Browse

Stay Connected