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Hybrid Technicien de production préparation milieu

Thermo Fisher Scientific · Seneffe, Belgien · Hybrid

  • Junior
  • Optionales Büro in Seneffe
Jetzt bewerben

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Preparation of Solutions and Media

  • Proactively implement all steps related to solution preparation, in alignment with established schedules.

  • Perform the following tasks: weighing, dissolving, pH measurement and adjustment, sterile filtration or autoclaving, aliquoting, labeling, and packaging.

  • Carry out depyrogenation and sterilization of production equipment.

  • Conduct routine microbiological and particulate monitoring of production areas.

  • Prepare consumables and solutions required for upcoming production steps.

  • Request and produce appropriate labels.

  • Coordinate the request and receipt of Collect & Go containers, and prepare pallets when necessary.

Operational Support

  • Participate in the theoretical and practical training of new team members.

  • Attend meetings essential to the role.

  • Apply the 5S methodology to maintain a clean and organized work environment.

  • Comply with and enforce current safety and biosafety regulations.

  • Ensure adherence to SOPs and GMP standards.

  • Provide regular updates on project progress as required.

  • Clean non-aseptic cleanrooms.

  • Take part in Line Clearance activities at the start, during, and end of campaigns.

Organizational Tasks

  • Independently manage day-to-day field logistics for production activities.

  • Handle temporary stock management (active components, consumables, raw materials) related to the project.

  • Oversee project-specific equipment setups.

  • Facilitate coordination with other platforms.

  • Ensure efficient management of local inventory.

Documentation Tasks

  • Ensure accurate data entry into management systems (e.g., SAP).

  • Maintain traceability of all operations through real-time completion of checklists and production documents, in accordance with good documentation practices.

  • Contribute to quality system management: review and draft SOPs and equipment setup sheets, implement CAPAs, manage deviations (in close collaboration with team and project leaders), complete logbooks and checklists, and review and compile batch records.