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Procesador Aséptico I TA

CSI · La Garita

Mid 🇬🇧 English
aseptic liquid filtration automated filling machines

Descripcion del puesto

About the role

We are seeking an Aseptic Processor I TA to join our production team in a clean‑room environment. You will be responsible for aseptic filtration and filling of IVF media, ensuring the highest standards of sterility and quality.

Key responsibilities

  • Perform aseptic liquid filtration and fill IVF media into bottles and micro‑vials using automated or manual equipment.
  • Clean and disinfect machine critical areas during start‑up, change‑over and shut‑down.
  • Transfer materials to and from the cleanroom while maintaining sterile barriers.
  • Prepare filling line sets, including component washing, assembly and sterilisation (dry‑heat or steam).
  • Follow safety rules, SOPs, cGMP, and company policies.
  • Conduct sampling and material identification for quality‑control inspections.
  • Complete batch records and documentation in accordance with GDP/GMP guidelines.
  • Maintain cleanliness and order of rooms, shelves and equipment.
  • Escalate issues promptly to lead or supervisor and support teamwork.
  • Perform additional duties as assigned.

Required profile

  • Secondary education (Bachillerato) completed.
  • Minimum 3 years experience in clean‑room environments (medical or pharmaceutical).
  • Experience with aseptic processes and bottle‑filling operations.
  • Basic understanding of microbiology principles related to medical devices or pharma.
  • Ability to read and interpret technical procedures, drawings and manuals.
  • Strong numerical skills for calculations of proportions, percentages, volume and weight.
  • Meticulous adherence to procedures and ability to work extended periods in clean‑room attire.
  • Basic English reading ability (B1 level is a plus).

Required skills

  • Aseptic liquid filtration
  • Automated filling machines
  • Manual filling processes
  • ISO clean‑room operations
  • Dry‑heat sterilisation
  • Steam sterilisation
  • cGMP compliance
  • GDP/GMP documentation
  • Batch record management
  • Quality‑control sampling

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Source : ats:oracle_hcm

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Publicado hace 1 mes

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CSI

La Garita