Über diese Manufacturing Operator Stelle bei 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 jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Supply Chain ManufacturingJob Sub Function:
Manufacturing Pharmaceutical Process OperationsJob Category:
Business Enablement/SupportAll Job Posting Locations:
Leiden, South Holland, NetherlandsJob Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Role Overview
The role is an experienced Operations Support Contributor responsible for executing routine tasks that support internal operational teams. The position ensures the accuracy, timeliness, and quality of deliverables by following established administrative processes and regulatory guidelines. The employee operates with professionalism, efficiency, and independent judgment, contributing to operational excellence while adhering to company policies, compliance standards, and continuous improvement practices.
Key Duties & Responsibilities
- Execute routine operational tasks to meet production targets under general supervision.
- Follow standard operating procedures (SOPs) to support processing of materials and/or pharmaceutical products.
- Ensure compliance with Good Manufacturing Practices (GMP), regulatory requirements, and company policies.
- Monitor resources, identify potential issues, and escalate concerns to leadership as needed.
- Maintain accurate records, track performance metrics, and identify gaps between targets and outcomes.
- Contribute to continuous improvement initiatives to enhance efficiency, quality, and safety.
- Take ownership of personal training and ensure completion of all required learning activities on time.
Requirements
- MBO-2 degree with at least 3 years of relevant experience, or 5 years of relevant experience with a non-related degree.
- Working proficiency (B1 level or higher) in Dutch or English.
- Basic proficiency in MS Office and routine use of business applications.
- Strong attention to detail with a quality-focused mindset.
- Positive attitude, adaptable, and able to manage shifting priorities.
- Understanding of GMP and regulatory environments is preferred.
- Willingness and ability to work in a shift-based schedule.
Here’s what you can expect:
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Application review: We’ll carefully review your CV to see how your skills and experience align with the role.
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Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
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Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
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Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA
Required Skills:
Preferred Skills:
Administrative Support, Agile Manufacturing, Analytics Dashboards, Chemistry, Manufacturing, and Control (CMC), Communication, Data Compilation, Data Savvy, Execution Focus, Gap Analysis, Good Manufacturing Practices (GMP), Operational Excellence, Plant Operations, Process Optimization, Process Oriented, Project Administration, Regulatory Compliance, Self-Awareness
The anticipated base pay range for this position is:
€35’000.00 - €53’360.00
Benefits:
In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.
*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
