Equipment Engineer Fill & Finish

Johnson & Johnson · Sassenheim, Netherlands

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 Manufacturing

Job Sub Function:

Manufacturing Pharmaceutical Process Operations

Job Category:

Professional

All Job Posting Locations:

Sassenheim, Netherlands

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

The Lenti Viral Vector (LVV) Facility: Janssen Biologics B.V., part of Johnson & Johnson, has launched a state-of-the-art production facility in Sassenheim. In this new facility lentiviral vectors are produced, which are used in the CAR-T treatments for multiple myeloma. The Centre of Expertise (CoE) is an essential support group in the LVV Facility.

The CoE is a critical team in the direct support of Operations when it comes to technical process and reliability of equipment. The CoE is key in clear translation of the developed process to a workable process and environment for the shop floor. The CoE always works against the high-quality standards and safety and compliance regulations that are applicable for LVV manufacturing. CoE is responsible for supporting the production teams with specialized and in-depth knowledge and skills in our production processes, GMP (Annex1), Digital & Technology, Materials and Single Use Items. The Centre of Expertise (COE) is a team of around 15 specialists.

The CoE team is one of 4 departments within the LVV facility and working with the Operations Department (OPS) which is responsible for the safe, compliant, efficient, and on time production and delivery of the batches (USP, DSP, F&F). Supported by a separate team with GMP specialists and the New Product Introduction (NPI) team to introduce new products or implement big process changes to existing GMP production processes.

We are searching for the best talent for Equipment Engineer Fill & Finish to be based in Sassenheim.

Join the LVV (Lentiviral Vector) Facility CoE — a small team of specialists supporting safe, compliant, and reliable LVV production used in advanced cell therapies. As Equipment Engineer Fill & Finish, you will own filling, labeling and visual inspection systems, help translate processes to the shop floor, and enable operations to run first‑time‑right.

As an Equipment Engineer Fill & Finish, you will:

  • Act as system owner for Fill & Finish equipment: provide hands‑on solving and production support to keep cGMP batches on schedule and compliant.
  • Translate technical and transfer requirements into procedures, training, and qualifications so operators can run equipment safely and reliably.
  • Monitor equipment KPIs (uptime, downtime, capacity, lifecycle) and propose high‑impact improvements for safety, quality, reliability, and cost.
  • Lead and coordinate short‑term change control and robustness actions (0–3 months), prioritizing tasks with operations, maintenance, and engineering.
  • Plan and implement test protocols, acceptance activities, and documentation updates to maintain validated states and production readiness.
  • Initiate and support cost‑saving and process‑improvement projects that improve reliability and ease of operation.

Qualifications/Requirements:

  • Bachelor’s degree or equivalent experience in biotechnology, biochemistry, biomedicine, process technology, or equivalent.
  • 3–4 years’ hands‑on manufacturing experience in biotechnology or biopharmaceutical environments.
  • Demonstrated knowledge in at least one area: Annex 1, drug product filling, visual inspection, or vial labelling.
  • Practical experience with cGMP environments and EHSS (safety) standards.
  • Strong communicator in English (B2 required); Dutch proficiency is a plus.
  • Proactive, organized team player with the ability to work independently, lead technical tasks, and collaborate across sites.

Here’s what you can expect:

  • Application review: We’ll carefully review your CV to see how your skills and experience align with the role.
  • 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.
  • 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.
  • 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 #LI_Onsite

 

 

Required Skills:

 

 

Preferred Skills:

Agile Manufacturing, Analytical Reasoning, Analytics Dashboards, Business Behavior, Chemistry, Manufacturing, and Control (CMC), Communication, Data Analysis, Data Compilation, Data Savvy, Execution Focus, Gap Analysis, Good Manufacturing Practices (GMP), Manufacturing Standards, Operational Excellence, Plant Operations, Process Optimization, Project Administration, Technical Credibility

  

 

The anticipated base pay range for this position is:

€44,700.00 - €70,840.00

 

 

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.

 

 

Hardware pay context

Based on 2,374 disclosed Hardware salaries on RoleSuite, the role pays a median of $135K/year, with most offers between $109K and $172K (10th–90th percentile: $91K–$207K).

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