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Manufacturing Specialist; Product Supply

Trabajo disponible en: 04810, Madrid, Andalucia, España
Empresa: ALK-Abelló A/S
Tiempo completo puesto
Publicado en 2026-09-12
Especializaciones laborales:
  • Control de Calidad
    Producción QC/QA, Analista de cumplimiento, Ingeniería de Calidad
  • Fabricación
    Fabricación farmacéutica, Producción QC/QA, Analista de cumplimiento, Ingeniería de Calidad
Rango Salarial o Referencia de la Industria: 42000 - 64000 EUR Anual EUR 42000.00 64000.00 YEAR
Descripción del trabajo
Puesto: Manufacturing Specialist (Product Supply)

Manufacturing Specialist (Product Supply)

Are you looking for an exciting opportunity to develop your manufacturing skills in a growing, international pharmaceutical company? At ALK, we are on a mission to improve the lives of people living with allergies, and we are seeking a dedicated and driven Manufacturing Specialist to join our Manufacturing Department
.

In this role, you’ll be the go‑to manufacturing specialist supporting three core areas: sterile filling, bulk manufacturing, and material preparation. This is a hands‑on, cross‑functional role for a problem‑solver who thrives on the shop floor, champions GMP excellence, drives continuous improvement and enjoys collaborating across teams.

Your key responsibilities:

The Manufacturing Technician supports sterile and non‑sterile production operations, ensuring safe, efficient, and fully compliant processes aligned with GMP and regulatory expectations.

Key responsibilities include:

  • Operational & Technical Support - Provide day‑to‑day technical support across sterile filling, bulk manufacturing, and material preparation. Operate and oversee critical aseptic manufacturing equipment such as ovens, autoclaves, SAS, RABS, and cleanroom systems.
  • GMP & Aseptic Compliance - Ensure proper execution of aseptic practices, gowning, line clearance, and environmental monitoring oversight. Support compliance with EU GMP Annex 1 requirements.
  • Issue Resolution & Investigation - Lead structured problem‑solving for deviations, equipment issues, and process failures. Drive robust CAPA and change control implementation.
  • Documentation Ownership - Maintain, update, and optimize manufacturing documentation including SOPs, batch records, work instructions, and risk assessments (FMEA).
  • Cross‑Functional Collaboration - Partner with QA, QC, Engineering, Supply Chain, Validation, and HSE during audits, investigations, media fills, and cleaning validation. Contribute to regulatory inspection readiness.
  • Equipment & Process Qualification - Support qualification and validation activities (IQ/OQ/PQ) for equipment and manufacturing processes.
  • Data Analysis & Continuous Improvement - Analyse performance data (downtime, rejects, EM trends, yield) to identify improvement opportunities. Implement practical improvements with operators and supervisors.
  • Training & Capability Building - Train teams in GMP, aseptic technique, standard work, and digital systems such as MES/e  and SAP. Promote safety‑and‑quality‑focused behaviours.
  • Material Management - Ensure material readiness through correct handling, segregation, sterilisation, FEFO/kanban application, and availability for sterile and non‑sterile operations.
  • Operational Excellence - Support 5S, visual management, and Gemba routines.

Your profile:

  • Degree in Pharmacy, Chemical/Biomedical Engineering, Biotechnology, or related discipline (Master’s is a plus).
  • 3–5 years’ experience in GMP pharmaceutical/biotech manufacturing, ideally with sterile/aseptic operations.
  • Strong knowledge of EU GMP (including Annex 1) and manufacturing best practices, data integrity, validation, and investigation methodologies.
  • Strong IT skills, especially in Microsoft Excel
    .
  • Experience with manufacturing systems (MES/e ), and ERP (SAP), plus quality systems (deviation/CAPA/change control).
  • Fluent Spanish and English; excellent technical writing and communication skills.

Your skills and attributes:

  • Hands‑on, calm under pressure, and comfortable across different manufacturing areas.
  • Meticulous attention to detail with a pragmatic, risk‑based approach to compliance and operations.
  • Structured problem‑solver with strong analytical skills; confident with data analysis and trending.
  • Collaborative and able to influence without authority; strong stakeholder management.
  • Proactive continuous improver;
    Lean/Six Sigma exposure (Green Belt desirable).
  • Location:

    C/ Miguel Fleta, 19 (Madrid, Spain).
  • Reporting line:
    Manufacturing Manager.
  • Work pattern: regular day shift with a flexible schedule.

We provide:

  • Competitive salary package
  • Career development opportunities and continuous training
  • Stable employment and a positive work environment
  • A comprehensive benefits package including health insurance, subsidized meals, and a pension plan.
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