Johnson & Johnson

Company Name: Johnson & Johnson
Job Title: Machine learning operations (MLOps) engineer
Job Description: 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

R&D Product Development

Job Sub Function

R&D Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations:

Turnhout, Antwerp, Belgium

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 Machine learning operations (MLOps) engineer to be in Beerse.

Purpose

At Janssen we strive to improve life and outcomes of millions of patients worldwide. Do you want to be a true pioneer and are you willing to join us in our journey towards the development of innovative therapeutics? If so, this MLOps engineer role could be a great opportunity to explore!

About The Department

The Global Pharmaceutical Product Development and Supply organization (PPDS) is within the Therapeutics development and supply (TDS) organization of Pharmaceutical Companies of Johnson and Johnson responsible for the development of Pharmaceutical Dosage forms with development centers located in the US, Asia, and Europe.

For the location in Beerse, Antwerp, Belgium we have an open position for a MLOps engineer.

Together with a complementary team of process engineers and formulation scientists, you will be responsible for strengthening our process and formulation capabilities for oral and parenteral solid and liquid dosage forms. The team is responsible for defining and developing predictive process models which enhance and fasten the scale up of the drug product process between different labs and production plants.

By means of data sciences and process modelling toolsets, it is our aim to fully understand the process behavior in order to deliver the best product and process at launch in an accelerated way..

You Will Be Responsible For

Join forces with our team of process engineers and play a crucial role in shaping the future of drug formulation and process development. Your responsibilities will encompass a diverse range of activities:
Design and develop robust data pipelines and databases to efficiently process and store large datasets, facilitating advanced analytics and machine learning operations
Develop and automate ETL processes for data extraction, transformation and loading
Collaborate with cross-functional teams to define data requirements and ensure the integration of data systems.
Create user-friendly front-end applications for data visualizations and automatic reporting.
Develop, implement and manage machine learning models to enhance process efficiency and quality
Implement best practices for model versioning, monitoring and tracking to ensure compliance with regulatory standards
Develop our process modelling toolbox of the future by leveraging your expertise in AI/ML and identify opportunities for the continued optimization of our predictive process models
Share your expertise with your colleagues and communicate in a clear way with your stakeholders to share your results and innovative ideas

Qualifications / Requirements

PhD or Master in data sciences, computer sciences, engineering or related field with 4+ years' experience.
Proven experience in MLOps or similar roles within the pharmaceutical, biotechnology or healthcare sectors.
Strong programming skills in languages such as Python, R or Matlab with a focus on data manipulation and ML frameworks (e.g. Tensorflow, PyTorch, Scikit-learn)
Experience with cloud platforms (e.g. AWS, Azure) for model deployment
Solid understanding of machine learning algorithms, model evaluation, preferably in the context of process development
Excellent problem-solving skills, with the ability to work collaboratively in cross-functional teams and communicate complex concepts to non-technical stakeholders.
The candidate is required to possess effective oral and written communication skills in English.

The position is fixed until 2026 with possibility to extend.

Turnhout, Belgium

Hybrid

04-04-2025

Company Name: Johnson & Johnson
Job Title: Commissioning and Qualification Engineer
Job Description: CAR-T QA C&Q Engineer

Location: Ghent
Working mode: Hybrid (Fully on-site during busy periods)
Duration: Contract running until the end of 2025 (opportunity for a contract extension)
Language requirements: Dutch and English
Hours: 40 hours per week
Pay rate range: Competitive hourly rate

The Janssen Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting a CAR-T QA C&Q Engineer for the CAR-T hub in Europe.

CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T-cells and are engineered to eliminate cancer cells expressing a specific antigen.

To support the CAR-T program in EMEA, Janssen is starting up two CAR-T manufacturing centres in the Ghent area (Belgium). The QC laboratories will be operated from the existing Janssen Beerse site.
The CAR-T QA C&Q Engineer is part of the CAR-T QA Qualification Team in Ghent. He/she will be responsible for review and approval of qualification and requalification activities, related to Facilities and Utilities (F&U) and Process Equipment at the Janssen/Legend Biotech facilities in Ghent.

roles and responsibilities
Will work closely together with the MAM (make asset management) and E&PS department and guard the qualification status of critical production assets by ensuring that all system critical aspects related to facilities & utilities, product and process requirements are identified; qualified and controlled by a mitigation plan and ensure that deviations related to equipment issues with possible impact on quality and/or compliance are evaluated, thoroughly investigated and that adequate corrective and/or preventive actions are defined and implemented
Will work closely together with the manufacturing department to approve new change controls and to ensure that deviations with possible impact on quality and/or compliance are evaluated, thoroughly investigated and that adequate corrective and/or preventive actions are defined and implemented
Will build a strong connect with different quality organizations
Will manage the compliance status of critical production (make) assets by means of review and approval of procedures e.g. calibration rationales, calibration master forms and completed calibration records, master data set-up, maintenance plans and follow up daily operations activities by review and approval of data integrity deliverables such as system audit trail and user access reviews
Approves qualification documents (change controls, master documents, protocols, reports, rationales, SOP’s, URS, IA, QSR, etc.) including discrepancies/events/non-conforming situations and related corrective actions (correction, CPA) occurring during execution of qualification activities.
Participates in system and process improvement / optimization projects and assure quality and compliance aspects and maintain a current knowledge of international regulations, guidelines and industry practices and become the QA process expert.

how to succeed
master’s degree in engineering with chemistry or analytical background or in pharmaceutical sciences
awareness of quality; have knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell therapy products and you see it as a challenge to defend our strategy and documents towards health authority inspections.
affinity with computerized systems, System parameter configurations and data management in critical production assets
ability to show and apply strong communication skills and are known as a great teammate who can work cross departmental in a continuous changing environment
thorough knowledge of Dutch and English, both orally and in writing
Strong analytical thinking, risk assessment and communication skills
Collaboration and teaming skills

benefits
This role offers a very competitive hourly rate. This contract will run until the end of 2025 and has a strong chance of extension.

you are welcome here
Johnson & Johnson Innovative Medicine is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine
Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.
Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.
We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

application process
We are looking to process the first round of applications within the next 2 working days.
We do not accept applications via email. The pay rate for this role will depend on how you are paid. Options are available.

Diversity, Equity & Inclusion
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.

Ghent, Belgium

Hybrid

15-04-2025

Company Name: Johnson & Johnson
Job Title: Data Scientist, AI/ML Drug Discovery
Job Description: 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

Data Analytics & Computational Sciences

Job Sub Function

Data Science

Job Category

Scientific/Technology

All Job Posting Locations:

Beerse, Antwerp, Belgium, Spring House, Pennsylvania, United States of America, Toledo, Spain

Job Description

AI/ML Senior Scientist in Drug Discovery Data Sciences

Next Generation Automation refers to the bidirectional coupling between automated lab equipment and Artificial Intelligence (AI). Through successive iterations, such closed-feedback loop systems facilitate the AI-driven design, execution and analysis of experiments and utilize a wealth of in silico methodologies including active learning, multi-parametric dynamic optimization, model predictive control, Model-based Design of Experiments, and others.

Within the Drug Discovery Data Sciences organization of Johnson & Johnson Innovative Medicine we have an open position for a senior scientist that will play a pivotal role in our strategic effort to transition automation into the next generation. To do so, the new member will collaborate within interdisciplinary teams comprising biologists, medicinal chemists, data scientists, computational chemists and IT experts across all therapeutic areas. They are expected to utilize their expertise and know-how to bridge the gap and close the loop between existing automation and in silico solutions and develop new modeling suites according to the needs of each project.

Role And Responsibilities

Co-develop system engineering plans for closed loop automation projects from PoC to production.
Develop and productionize the in silico suites by using AI/ML and other appropriate modelling methodologies.
Actively participate in evaluation of third-party solutions.
Work closely with IT, engineering and Lab-tech to implement solutions.
Communicate results in audiences with heterogeneous background.

Requirements

A PhD with an AI/ML publication track record.
Previous experience with Process or Lab Automation.
Familiarity with Model Predictive Control and DOEs or similar mathematical capabilities.
Knowledge of Python development and affinity with AWS (or similar cloud environments).
Strong interpersonal, organizational and communication skills.
Motivation to be part of a team that celebrates diversity and offers an inclusive working environment where creativity and innovation can thrive.

Beerse, Belgium

Hybrid

23-04-2025

Company Name: Johnson & Johnson
Job Title: CAR-T Asset Engineer
Job Description: 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 Engineering

Job Sub Function

Manufacturing Engineering

Job Category

People Leader

All Job Posting Locations:

Beerse, Antwerp, Belgium, Gent, East Flanders, Belgium

Job Description

This position will be part of the CAR-T Asset Engineering team within the Make Asset Management organization (MAM). The Asset Engineer is responsible for providing technical expertise on the lab equipment (asset) of the CAR-T process as well as performing Commissioning and Qualification activities within the cGMP Clinical and Commercial Cell Therapy Manufacturing plants serving Ghent and Beerse sites. The role will be a key contributor to ensure flawless operation and asset management projects in close collaboration with the different project organizations, vendors, sites, and stakeholders.

Imagine empowering the body’s own immune system to fight cancer. That’s exactly what CAR-T therapy does. It uses a patient’s own T-cells, reprogramming them to target and destroy cancer cells. This advanced therapy holds the promise to change lives — and you can be part of that journey !

Key Responsibilities

Manages multiple business requests and/or small projects equipment related
Supports in planning and execution of C&Q activities
Provide SME knowledge and support for troubleshooting scenarios
Sustains continuous technical improvements around our Asset base
Drive to solutions by coordinating with other internal departments and/or outside suppliers
Supports technical investigations detected during C&Q activities.

Qualifications

Education:

A minimum of a Master’s Degree in Science, Engineering, Bioengineering or equivalent technical discipline is required.

What You Bring

6+ years of experience in the pharmaceutical manufacturing / engineering environment
Experience in commissioning & qualification (C&Q) is a Plus.
A hands-on, solution-oriented mindset.
A strong understanding of GMP guidelines and experience with audits or inspections.
A collaborative and open approach — you thrive on teamwork and knowledge sharing.
Demonstrate ownership and strong analytical/communication skills
Fluent in English (written and spoken), Dutch language is a Plus

What We Offer

A meaningful role where your work has a direct impact on cancer patients’ lives.
A supportive environment that values your growth, creativity, and contributions.
A diverse and inclusive workplace where everyone can thrive.

Ghent, Belgium

Hybrid

23-04-2025

About the Company

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