Responsibilities
* Independent coordination (receiving, input, storage, disposal, document management) of complaint samples according to cGMP standard.
* Evaluating Temperature Excursions to assess if products remain safe for human use Working reliably according to standard work instructions
* Documentation of sample information in the Johnson & Johnson Complaint Database.
* Responsibility for laboratory equipment and ensuring timely maintenance measures
* Check of product serialization and product decommissioning state
* Coordinating and assisting with general lab work and lab activities in QA Complaint Laboratory
* Author and own laboratory work instructions
* Support additional project team activities and/or investigations, and participate in process improvement activities and projects
Qualifications
* Strong written and verbal communication skills in English and German are required.
* Effectively manages work & time to produce desired outcomes (time management).
* Continuous interaction and coordination with internal stakeholders. Investigative & analytical critical thinking skills.
* Experience in regulated industry is preferred. Completed training as a laboratory assistant (CTA, BTA) is an advantage.
#J-18808-Ljbffr