Manufacturing Operator

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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:
Business Enablement/Support

All Job Posting Locations:
Sassenheim, Netherlands

Job Description:

We are looking for the best Manufacturing Operators for our USP/DSP and Fill and Finish departments in Sassenheim, Netherlands!

Join our fully digital Lenti Viral Vector Facility in Sassenheim, producing vectors for multiple myeloma treatment impacting 160,000 patients worldwide.

As we prepare for commercial production in mid-2026, we're looking for Manufacturing Operators (USP/DSP/F&F) to support cell expansion, virus production, purification, and automated filling under GMP and BSL2 conditions.

Build your career at the forefront of innovation in a collaborative environment, with strong growth opportunities through training, mentoring, and clear career paths

As a Manufacturing Operator, you will Support the installation and operation of new equipment, writing job breakdown sheets for training and work instructions.

Collaborating in the execution of the daily task and the supporting activities of the department according to procedures and detailed schedule.

Perform process and GMP documentation activities raise process deviations, notice process gaps, and tackle them, train operators.

Contribute to continuous improvement of processes and procedures Work safely and compliantly in line with GMP, EHS, and quality standards

Qualifications / Requirements:


* Preferably an MBO 4 or HBO in laboratory & biotechnology, biochemistry, biomedicine, process technology, allround laborant OR equivalent education level with proven experience in biotech or biopharma manufacturing.


* Hands-on expertise in a BSL2 environment, focusing on cell culture, virus propagation, purification, or Fill & Finish, adhering to GMP and EHS standards.


* Strong English communication skills, with the ability to analyse complex situations and maintain high accuracy and independence.


* Adaptable teammate with a proactive approach, ready to tackle challenges and work flexible shifts.

Your Benefits:


* 12-month contract incl.

1 month ...