QC Environmental Logistics Analyst (2nd Shift)

7555-Janssen Pharmaceutica NV Legal Entity; Geel; Sur place; EUR 43 000 - 59 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Résumé du poste

Johnson & Johnson is seeking an EM/Logistic Analyst for the CAR‑T Europe program. You will oversee Environmental Monitoring sample handling, processing and analysis, plus the logistics of Drug Product samples and critical reagents. The role involves QC administration and ensuring GMP‑compliant lab operations.

Work is in a two‑shift system (early and late) with a temporary appointment to start. You will collaborate with cross‑functional teams to safeguard accurate sampling and documentation

Qualifications

• 2 years of experience in a cGMP environment within Environmental Monitoring, logistics or a similar role.
• Experience with Environmental Monitoring tests is a strong plus.
• Good knowledge of GMP guidelines and quality/compliance procedures.
• Strong administrative skills with attention to detail and documentation.

Responsabilités

• Receive, unpack, incubate and read Environmental Monitoring samples per GMP guidelines.
• Perform Environmental Monitoring tests and correctly record results.
• Receive, process, store and manage Drug Product samples at various temperatures (-120°C, -80°C, 2-8°C).
• Coordinate internal transport of Critical Reagents and support material flow.
• Handle QC administrative tasks, including processing COA results in eLIMS for gowning, cleaning and other consumables.
• Support laboratory investigations, CAPAs, safety initiatives and participate in lab meetings.

Connaissances

cGMP experience

Environmental Monitoring

Logistics

MS Office

Documentation

Outils

Microsoft Office (Outlook, Excel, Word, PowerPoint)

Description du poste

Johnson & Johnson is seeking an EM/Logistic Analyst for the CAR‑T Europe program. You will oversee Environmental Monitoring sample handling, processing and analysis, plus the logistics of Drug Product samples and critical reagents. The role involves QC administration and ensuring GMP‑compliant lab operations.

Work is in a two‑shift system (early and late) with a temporary appointment to start. You will collaborate with cross‑functional teams to safeguard accurate sampling and documentation