Supervisor Plant Management - Sassenheim, Nederland - Johnson & Johnson

Johnson & Johnson

Geverifieerd bedrijf

Sassenheim, Nederland

1 week geleden

Geplaatst door:

Daan Van den Berg

werver van beBee

Beschrijving

Functie:
(Senior) Manufacturing Supervisor

Kopzin:
Would you like to be directly involved in supporting a new process that can change people's life?

Then keep reading

Project Pollux is the establishment of a new Janssen Supply Chain Lentiviral Vector (LVV) production facility in Sassenheim, the Netherlands to be organized as a new business unit for Janssen Biologics (JBV).

This biologics manufacturing facility is intended to become a key supply option for commercial LVV in support of the global Janssen BCMA CAR-T program for multiple myeloma, a disease affecting ~160,000 patients annually.

The production facility is currently being qualified with the following milestones in the long-lead project plan:

Facility and production equipment qualification
Handover of Facility from project team to Operations
Production of Engineering batches
Producing of Qualification batches
Licence approval, start Commercial manufacturing.

Are you energized to support a new organization within a global company? Do you want to contribute to improve the life of patients? Do you have a strong passion for people? Then this is your job

For this project Janssen Biologics is recruiting a Manufacturing Supervisor to work within the Operational Readiness department to support this new facility now and in the future.

Operations organization
In full operation, Operations manufactures the Lenti Viral Vector for our customers. This process is following different steps from cell expansion, virus production and clarification to automated filling and labelling. The process is performed under strict GMP and BSL2 conditions.

During the project the team is preparing the plant for operations and supporting the technology transfer from R&D by developing procedures and training, and the team will produce test and qualification batches.

Job Summary:

As Manufacturing supervisor, you will lead a group of specialists and senior manufacturing operators (in the areas of Training, GMP, Digital Technology, Single Use Items and Consumable materials) within the LVV operations department.

You work closely with the other functions, Manufacturing Supervisors and Manufacturing Process Specialists, and Process Engineers.

As supervisor, you will further build on and maintain the completely new organization for de LVV facility.

This means you will participate in the recruiting process for the operations department of the LVV facility, manage and coach the operations team during the phase III and commercial production of the Lenti Viral Vector.

As supervisor you are part of the management team of the LVV and reports to the Operations Manager.

The manufacturing supervisor gets the best out of his or her people and is responsible for delivering a high-quality product within the applicable standards in the field of safety and compliance.

The responsibilities and the impact YOU will have:

The execution of the activities within the operations support team, according to the set standards (cGMP, EHSS, Process Excellence) and continuously improves it.
As a people manager, ensuring that there is a stable team with a positive constructive atmosphere. You motivate, coach and support your employees to get the best out of your team.
Performing all people management task e.g. holds the 5 conversations, recruitment and selection, absenteeism guidance, coaching, propagating the CREDO values.
Sufficient training (process, process excellence, etc.) and occupation of the team members.
Supporting and leading to reaching the objectives of the LVV facility.
Setting priorities and aligning them with the departments involved, constantly assessing, and improving the efficiency of the processes and the team, so that the production systems, the production facility and the resources are optimally utilized.
An effective communication between the various locations, peers (internal / external / JBV) and promotes cooperation and synergy in this.
Supervising activities carried out by third parties (training, qualifications, etc.) in your responsible area.

Qualifications:

We would love to hear from YOU, if you have the following essential requirements:
Capabilities identified as priority for our Workforce of the Future are:

Digital & Technology
Change Leadership
Critical Thinking & Problem Solving
Process knowledge & expertise
End to End mindset

Qualifications:

Bachelor's degree in biotechnology, biochemistry, biomedicine, process technology (or equivalent education).
68 years' experience in a biotechnology or biopharmaceutical industry environment.
Demonstrable organizational and managerial capacities.
Demonstrable people management qualities.
Excellent communication skills.
Good command of English in word and writing
Demonstrated EHS and GMP awareness.
Experience with Lean methodology, Certified Green Belt.

Key Competencies: