Manufacturing Coordinator (H/F/X)

White Raven - WHITE RAVEN; Luik; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

White Raven manufactures in Liège, Belgium and seeks a Manufacturing Supervisor to lead aseptic floor operations on a Cytiva SA25 robotic isolator platform. You will work hands-on with operators to execute GMP batches, engineering runs and process studies in a Grade C cleanroom.

You will train and qualify operators, ensure GMP/GDP compliance, and collaborate with the Manufacturing Coordinator and Project Manager on campaigns and changeovers.

Qualifications

• Experienced aseptic manufacturing professional with GMP discipline.
• GMP and aseptic expertise required; technical leadership without a formal management layer.

Responsabilités

• Run day-to-day aseptic filling in a fully robotic isolator platform.
• Own floor execution of GMP batches, engineering runs, and process studies.
• Review batch records for GMP and GDP compliance before hand-off to Quality.
• Collaborate with Manufacturing Coordinator on daily production and back-up roles.
• Plan manufacturing contribution to customer projects with project managers.
• Author and review manufacturing docs; maintain BOMs and routings in ERP.
• Ensure GMP adherence and maintain electronic documentation (eBMR, Odoo, QMS).
• Contribute to APS program and monitor process performance (RFT, OEE).
• Train and qualify operators on equipment, procedures, and GMP requirements.
• Lead or support continuous improvement initiatives (5S, Kaizen, DMAIC).
• Investigate deviations and act as CAPA/Change/Task Owner when assigned.
• Lead risk analysis sessions following standard methodologies.
• Collaborate with client auditors and regulators during audits.

Connaissances

GMP discipline

Aseptic expertise

Technical leadership

Outils

Odoo ERP

Scilife QMS

Description du poste

As aManufacturing Supervisor,you will join the Manufacturing team and report to the Head of Manufacturing.This is a hands-on, floor-based role: you will work side by side with the production operators to manufactureGMP batches, engineering runs and process studies on our Grade C cleanroom and Cytiva SA25 robotic isolatorplatform.

The role carries no hierarchical management of the operators. You lead the floor technically: you set up the line,you drive the batch, you train and qualify the team on the equipment and the procedures, and you are the personthe operators turn to when something does not look right. You will work as a close duo with the ManufacturingCoordinator, each acting as the other's back-up.

Role & Responsabilities

• Run day-to-day aseptic filling and formulation activities on the Cytiva SA25 fully robotic, gloveless isolatorplatform (setup, formulation, filling, post-filling, decontamination), on the floor with the operators.
• Own the floor execution of GMP batches, engineering runs, process studies and media fills: readiness check,line clearance, in-process controls, batch closure.
• Review executed batch records for GMP and GDP compliance before hand-over to Quality.
• Work as a duo with the Manufacturing Coordinator on the daily running of the production floor, and act as theother's designated back-up during absences.
• Plan the manufacturing contribution to customer projects with the Manufacturing Coordinator and the ProjectManager (campaign slotting, changeover readiness, material lead times).
• Author and review manufacturing documentation (Master Batch Records, work instructions, setup and lineclearance documents), and create and maintain manufacturing articles, BOMs, and routings in the OdooERP.
• Ensure strict GMP adherence in all production activities, including GDP-compliant electronic documentation(eBMR, Odoo, Scilife QMS).
  Contribute to the APS program (documentation and floor execution) and monitor process performance (RFT,OEE, deviations, contamination rate).
• Train and qualify the production operators on equipment, procedures and GMP requirements, and keep theiraseptic qualification current with the Head of Manufacturing.
• Lead or support continuous improvement initiatives (5S, Kaizen, DMAIC, standard work) and keep SOPscurrent.
• Investigate deviations and non-conformities within scope; act as CAPA / Change / Task Owner whenassigned.
• Lead risk analysis sessions following standard risk assessment methodologies.
• Collaborate with client auditors and regulators during audits and inspections.

Ideal Candidate

We are looking for an experienced aseptic manufacturing professional who wants to stay on the floor:GMPdiscipline,aseptic expertiseand
technical leadershipwithout a management layer.