Training Supervisor - Raritan, United States - Legend Biotech

Legend Biotech Raritan, United States

6 days ago

Description

Legend Biotech is seeking

Training Supervisor - Operations as part of the

Training

team based in

Raritan, NJ.

Role Overview

The position will be responsible for supervising the training team who lead training activities for the overall plant team members who support cGMP Clinical and Commercial Cell Therapy Manufacturing.

This individual will oversee the Training team members in collaboration with department management in Operations and Quality to support personalized cell therapy production through safe and compliant operations according to cGMP requirements.

This individual will support organization build and rampup of clinical production and facility approval of a state-of-the-art cell therapy facility for commercial launch and sustained production.

The role will require technical experience, effective communication, coordination and collaboration across relevant cross functional groups to enable robust production, testing and release of product to patients.

Key Responsibilities

Leads, directs, coaches and develops a holistic, effective training program for all plant functions and personnel that support daily clinical production and strategically prepares for commercial supply of a CAR-T product.

Manages training team to plan, coordinate, prepare and deploy training curriculum.

Perform training assessments for new and updated procedures.

Oversee and schedule training skill checks and qualifications.

Support evaluation of appropriate compliance courses.

Leads and works with training team to manage training requirements for new hires.

Work collaboratively with functional leads for procedure alignment based on roles.

Serve as subject matter expert for Compliance & Training systems.

Make recommendation for future system upgrades.

Troubleshoot problems reported by system users.

Knowledge of LMS system.

Maintain and report quality training metrics.

Prepares information for internal and external audits.

Requirements

A minimum of a Bachelor's Degree in Science, Information Science or equivalent technical discipline is required.

A minimum of 6 years relevant work experience is required.

It is preferable that the candidate have experience working within an aseptic manufacturing facility, preferably in training/system applications, quality systems, or learning management systems.

Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products as well as knowledge of Good Tissue Practices.

Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members.

Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability.

Advanced computer skills and practical knowledge of MS Office Suite, SharePoint, and other related systems.

Good verbal and written communication skills.

Excellent organizational skills.

Ability to effectively prioritize and execute tasks in a fast-paced environment.

Works well in a team-oriented, collaborative environment.

The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision.

Proactive and continuous improvement oriented.

Ability to lead with influence.

cGMP manufacturing.

Able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members.

Strong analytical, problem solving and critical thinking skills.

Project management.

Change management.

Transparent, Passionate, Fearless and Accountable.

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