Open for applications

TWI Writer

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About the vacancy

Engineering
Manufacturing Engineering
Process Engineering
Quality (Engineering)
General
Manufacturing
Quality
Quality Systems
Sales
Communication
IT
Data & Analytics
Staff
Administrative
Educator
Expert Vocational Training (MBO) Permanent Full time 38,300.00 to 61,410.00 Netherlands

About Your Next Job

We are searching for the best talent for TWI Writer to be based in Groningen.


We are looking for a hands-on technical writer to create and maintain manufacturing work instruction documentation that follows the TWI methodology and supports continuous improvement. You will help make work clear, usable, and auditable so operators and engineers can perform consistently and safely!


This role sits within the Manufacturing Process Improvement function and works closely with operators, engineers, quality, training, and document control to turn time-study findings and process mapping into practical, implemented documentation changes.


About Your Tasks and Responsibilities

As a Quality Control Analyst, you will:

  • Write and maintain manufacturing work instruction documentation (WV and JBS) that follows TWI methodology and meets operational quality standards.
  • Implement documentation updates through Agile workflows, coordinating roll-out with training and document control to ensure timely adoption.
  • Map work processes and act on opportunities identified in time studies to drive improvements in cost, yield, cycle time, or space usage.
  • Collect, analyze, and maintain a database of process improvement activity and issues, and communicate findings to Business Excellence engineers for resolution.
  • Deliver classroom training for operators, support training follow-up, and advise on production document strategy to embed and sustain changes.


About Your Skills and Experience

Qualifications/Requirements:

  • Relevant technical education or equivalent practical experience in manufacturing, engineering, or a related field.
  • Proven experience writing and maintaining manufacturing work instruction documentation using TWI methodology.
  • Comfortable working within Agile implementation approaches and following administrative processes to ensure accuracy, timeliness, and quality.
  • Strong collaboration and communication skills with a track record of engaging operators, engineers, quality, training, and document control to achieve outcomes.
  • Experience collecting and analyzing process data, maintaining improvement databases, and a willingness to demonstrate the organization’s leadership imperatives and Credo.

Preferred Skills:

Accountability, Administrative Support, Agile Manufacturing, Chemistry, Manufacturing, and Control (CMC), Communication, Data Gathering and Analysis, Detail-Oriented, Document Management, Goal Attainment, Good Manufacturing Practices (GMP), Issue Escalation, Plant Operations, Process Control, Process Optimization, Process Oriented, Quality Management Systems (QMS), Quality Standards, Quality Systems Documentation, Time Management


You are eligible to work in EU

We only accept applicants who are eligible to work in the EU


Contact person

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At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com



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