Join as an Operational Excellence Trainer responsible for onboarding and retraining in Manufacturing, Production Support, and Quality Control. You'll work on introducing cell and gene therapy processes and ensuring standardized training while upholding top GMP standards. Key roles include planning training sessions, identifying training bottlenecks, and coordinating specific process trainings. This is a full-time on-site position where you'll also guide and support Biotech and QC associates. English fluency is essential. Read on to learn why this position could be your next career move.

Over het bedrijf

Panda International

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The Operational Excellence Trainer is responsible for providing on-boarding and periodical retraining to Manufacturing, Production Support or Quality Control Operators. Training encompasses, but is not limited to, introduction training, processing activities linked to cell and gene therapy products manufacturing, production support activities, QC assays and for-cause trainings.

The Operational Excellence Trainer is responsible for reporting potential training bottlenecks in link with the Manufacturing Training Coordinator and Head of OE.

The activities of the Operational Excellence Trainer facilitate lean and standardized training, while maintaining the highest level of GMP adherence.

Role:

In accordance with the training schedule and the Manufacturing Training Coordinator, plan and provide Manufacturing, Production Support or Quality Control.
Track and report on training plan adherence.
Report training bottlenecks and opportunities for improvement to streamline training activities.
Coordinate Mock run, Unit Operation or equipment training related to a specific process or processing step.
Provides training to contractors or visitors entering the GMP area.
In link with the aseptic trainer, ensures best aseptic practices are adhered to, actively participates in continuous improvements and organizes follow-up.
Provide strong guidance to Biotech, Production Support and QC associates on project specific and general procedure trainings.
Interacts constructively with other departments.
Acts as a role model on GMP compliance.
Ensures full awareness on latest revision of SOPs/batch records.

Notes:

Full onsite position in GELEEN, Netherlands.
Fluent English required.
Dutch is an asset.
Degree in Life Sciences or Biology.
Minimum of 3 years’ experience in a GMP environment.

Interested? Send your CV to Daria at via de button "Solliciteer nu" op deze pagina. or call +31202044502 for more info.

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