Training Specialist (GMP Manufacturing)

Operational Excellence Trainer | GMP Manufacturing Training Job Description A life sciences manufacturing organisation is seeking an Operational Excellence Trainer to support onboarding and periodic retraining for Manufacturing, Production Support, and Quality Control operators within a GMP environment. The role focuses on delivering structured training programs related to cell and gene therapy manufacturing processes, production support activities, QC assays, and operational procedures while ensuring the highest standards of GMP compliance.

In this role, you will work closely with the Manufacturing Training Coordinator and Head of Operational Excellence to plan and deliver training in line with the established training schedule. You will support standardized and lean training processes, coordinate mock runs and unit operation training, and ensure operators remain fully trained on the latest SOPs and batch record revisions. The Operational Excellence Trainer will also identify and report training bottlenecks, provide guidance to operational teams, and contribute to continuous improvement initiatives related to training and operational practices.

Qualifications

Degree in Life Sciences or Biology

Minimum of 3 years’ experience in a GMP environment, ideally in a training-related role

Experience working within Manufacturing, Production Support, or Quality Control environments

Knowledge of GMP requirements and compliance within a pharmaceutical or biotechnology setting

Experience delivering onboarding and periodic retraining for operational staff

Ability to plan and deliver training activities in alignment with training schedules

Experience coordinating mock runs, unit operations, or equipment‑related training activities

Ability to guide and support Biotech, Production Support, and QC associates on procedural and project‑related training

Strong understanding of SOPs and batch record management and ensuring awareness of latest revisions

Strong communication and collaboration skills with the ability to interact constructively across departments

Ability to act as a role model for GMP compliance and best practices

Preferred Requirements

Dutch language skills are considered an asset

Experience supporting training activities related to cell and gene therapy manufacturing processes

Familiarity with aseptic practices and participation in aseptic training or related improvement initiatives

Experience providing training to contractors or visitors entering GMP environments

Ability to identify training bottlenecks and contribute to continuous improvement of training programs

Practicalities Start Date: ASAP

Location: Geleen, Netherlands

Work Model: Full onsite position

Scope: Training support for Manufacturing, Production Support, and Quality Control teams within a GMP environment.

Interested? Send your CV to Miguel Gomes at

m.gomes@panda-int.com

or call

+31 (0)20 2044 502 / +41 (0)44 5514 407

to discuss the opportunity.

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