Manufacturing Operator

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

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:

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

We are searching for the best talent for a Manufacturing Operator to be in Sassenheim, Netherlands!

Join our team at the new fully digital Lenti Viral Vector Facility in Sassenheim, aimed at producing Lenti Viral Vectors for multiple myeloma treatment, impacting 160,000 patients worldwide. As we prepare for commercial production starting mid-2025, Janssen Biologics is seeking a Manufacturing Operator (USP/DSP/F &F) for our Operational Readiness team. You'll be essential in supporting facility operations, which include cell expansion, virus production, purification, and automated filling under GMP and BSL2 conditions. If you're passionate about innovation and teamwork, we want you to be part of this groundbreaking opportunity! Check out where we are located

Check out what your future workplace as an operator looks like by clicking here.

About the departments:

Department: Upstream Processing (USP)
The USP department focuses on the culturing of cells and infecting them with a virus. The team operates on an 8/7 shift roster. Core tasks include:

• Culturing and inoculation of cells in Shaker Flask and Wave bag (e.g., cell count, dilution, sampling)
• Daily monitoring of cell culture including in-process testing (e.g., cell count, pH)
• Preparing transfection mix (process additions) and executing transfection
• Preparing Benzonase solutions (process additions)
• Harvesting SUB and clarifying the harvest
• Sample handling for the USP department

Department: Downstream Processing (DSP)
The DSP department is responsible for the purification of Lenti Viral Vectors using various techniques. During the project phase, you will work normal weekdays. The DSP team will consist of 10 operators on a day shift roster. Core tasks include:

• Purification using Ion Exchange chromatography
• Sterile filtration, including PUPSIT filter integrity testing
• Ultrafiltration and diafiltration
• Sample handling for the DSP department

Department: Fill and Finish (F&F)
The F&F department is responsible for the final filling and preparation of the product for freezing and storage. During the project phase, normal weekdays will be worked. Initially, the F&F team will consist of 3 sub-teams, each with 4 operators, primarily on a day shift roster, with 2 late shifts every three weeks. Core tasks include:

• Preparation of isolator and filler
• Filling of product in a Grade A isolator
• Aseptic working in an isolator with an automated filling robot
• Visual examination of product vials
• Labelling of vials and storage of the product in downstream freezers

You will be responsible for:

• 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 a detailed schedule.
• Perform process and documentation activities” raise process deviations, notice process gaps, and tackle them, train operators.
• Continuous improvement of work process and procedures.

Qualifications/Requirements:

• Preferably an MBO or HBO in biotechnology, biochemistry, biomedicine, process technology (or equivalent education) 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 analyze complex situations and maintain high accuracy and independence.
• Adaptable teammate with a proactive approach, ready to tackle challenges and work flexible shifts.

Ready for the next step in your career? Apply now!#RPOAMS