Open for applications

Manufacturing Supervisor - Technical Process and Compliance

logo of Johnson & Johnson

About the vacancy

Engineering
Manufacturing Engineering
Quality (Engineering)
General
Manufacturing
Quality
Repair & Maintenance
Staff
Procurement & Supply Chain
Project Management
Expert Associate Degree (HBO) Permanent Full time 44,700 to 70,840 Leiden, South Holland, Netherlands

About Your Next Job

We are searching for the best talent for Manufacturing Supervisor - Technical Process and Compliance to be based in Leiden.


We are looking for a hands-on Manufacturing Supervisor who will ensure safe, compliant, and efficient production while owning technical processes and driving continuous improvement. You will support a focused production team and collaborate closely with other supervisors, Engineering, Quality, and Maintenance to meet the Master Production Schedule and maintain high standards of cGMP and safety!


This role emphasizes technical ownership — from supporting new product and equipment introductions to leading investigations and process improvements — and requires strong communication in English and Dutch to work effectively across teams.


About Your Tasks and Responsibilities

As a Manufacturing Supervisor - Technical Process and Compliance, you will:

  • Own technical process performance for assigned areas, acting as the subject-matter expert and ensuring compliant, robust production outcomes.
  • Lead and contribute to deviations, root-cause investigations, and CAPA activities to resolve issues and prevent recurrence.
  • Support new product and equipment introductions by providing clear User Requirement Specifications, coordinating qualifications, and updating SOPs and work instructions.
  • Ensure accurate, timely GMP documentation and train operators on correct equipment use, documentation practices, and process controls.
  • Identify and drive data‑driven process and equipment improvements, partnering with Engineering and other stakeholders to implement changes.
  • Assign and coach operators, monitor team performance against the Master Production Schedule, and take ownership of operational metrics and corrective actions.


About Your Skills and Experience

Qualifications/Requirements:

  • HBO level education or equivalent practical experience in a technical or scientific field.
  • Minimum 3 years of relevant manufacturing experience, preferably in the medical device industry or medical field.
  • Strong knowledge of cGMP, EHS & Safety requirements and experience with Six Sigma or process‑excellence methodologies.
  • Proficient with Excel, Windows, and ERP systems, and able to collect and analyze data to inform decisions.
  • Fluent in English and Dutch with clear verbal and written communication and stakeholder presentation skills.
  • Collaborative leader who coaches others, manages a defined team, sets priorities, and supports continuous improvement.


You are eligible to work in EU

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


Contact person

logo of Johnson & Johnson

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



Share this vacancy

Is it OK if we use cookies?

We use cookies to make our website and advertisements more personal and relevant. If you do not agree, we will only place functional and analytical cookies