EM/Logistic analyst, QC CAR-T Europe

Johnson & Johnson Co.; Beerse; On-site; EUR 55,000 - 75,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave (min 12 weeks)

Bereavement leave

Caregiver leave

Volunteer leave

Job summary

Johnson & Johnson Beerse site is seeking an EM/Logistic analyst for the QC CAR-T Europe hub. The role focuses on Environmental Monitoring sample shipments, incubation, and read-out of results within GMP guidelines.

Based in Beerse, you will handle drug product shipments, sample storage across temperatures, and support CAPAs and investigations while maintaining safety and compliance in a fast-paced environment.

Qualifications

• Minimum two years of experience in a cGMP compliant EM and/or logistics function.
• Experience in Environmental Monitoring testing is a plus.
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, PowerPoint).
• Excellent written and oral communication skills are required.

Responsibilities

• Environmental Monitoring testing: Receival and unpacking of the shipment
• Incubation
• Read-out of results
• Perform EM testing in compliance with all specifications and GMP regulations
• Drug Product shipments, receival, unpacking and storage, including assigning storage locations for samples across temperatures
• On-site transport of Critical Reagents
• Copy of COA results in eLims for gowning, cleaning and other consumables
• General administrative QC tasks
• Maintain a safe work environment in compliance with regulations
• Support laboratory investigations and CAPAs
• Provide input to functional laboratory meetings

Skills

Communication

MS Office

Tools

Microsoft Excel

Microsoft Word

PowerPoint

Outlook

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 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:

Non-Standard

Job Sub Function:

Workday Associate B

Job Category:

Non-Standard

All Job Posting Locations:

Beerse, Antwerp, Belgium

Job Description:

Position Title: EM/Logistic analyst, QC CAR-T Europe

The Janssen Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting an EM/Logistic analyst for the QC CAR-T hub in Europe. The position will be based in Beerse Belgium.

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 has built two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories are located on the existing Janssen Beerse site.

The EM/Logistic analyst, QC CAR-T Europe is responsible for shipment of Environmental Monitoring samples, Drug Product samples and Critical Reagents. Next to that also the incubation and read-out of Environmental Monitoring samples will be part of your responsibilities. All activities should be following the applicable procedures, standards, and GMP regulations.

This job will be in a 2-shift regime: Early/Shifted late (6:00h-14:00h and 12:00h-20:00h)

Major Responsibilities:

• Environmental Monitoring testing: Receival and unpacking of the shipment
• Incubation
• Read-out of results
• Perform EM testing in compliance with all applicable specifications, procedures, GMP regulations
• Drug Product Shipments, receival, unpacking and storage, including assigning the right storage locations to the different samples for all different temperature conditions (-120°C/-80°C/2-8°C)
• On-Site transport of Critical Reagents
• Copy of COA results in eLims for gowning, cleaning and other consumables
• General administrative related QC tasks
• Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations
• Support laboratory related investigation records and CAPAs
• Provide input to functional laboratory meetings

Qualifications:

• A minimum of two (2) years of experience working in a cGMP compliant EM and or logistic function is required.
• Experience in Environmental Monitoring testing is a plus.
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) is required.
• Excellent written and oral communication skill are required

The anticipated base pay range for this position is:

€0.00 - €0.00

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 re