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Senior Reliability Engineer (m/w/d) (EN)

[16379]
Reliability, CMMS

Project title: Senior Reliability Engineer (m/w/d) Type of employment: Payroll Industry: Pharma Skills: Reliability,CMMS Project start: asap Project duration: 31.03.2026 Location: Neuenburg, Schweiz Home office working is acceptable but not on a full time basis Responsibilities ·Improve equipment and system reliability by applying reliability engineering principles in a cGMP-regulated biotech environment. ·Analyze maintenance data to reduce downtime and optimize maintenance strategies, including preventive and predictive programs. ·Lead root cause analyses (RCA), implement corrective/preventive actions (CAPAs), and support audit responses. ·Define equipment importance, develop and update maintenance plans and SOPs, and ensure the effectiveness of maintenance programs. ·Manage CMMS data, spare parts lists (BOMs/EPLs), and monitor equipment performance through trend analysis and KPIs. ·Support capital projects, collaborate across departments (production, quality, safety, engineering), and ensure regulatory compliance (GMP, FDA). ·Deliver training, promote reliability concepts, and maintain accurate documentation and vendor materials. ·Drive continuous improvement initiatives for maintenance effectiveness and cost optimization. Qualifications ·Experience in a GMP-compliant environment with strong knowledge of operational maintenance practices. ·Proficient in root cause analysis tools (FTA, RCA, RCFA) and data-driven decision making. ·Working knowledge of CMMS systems such as JD Edwards or SAP. ·Strong analytical, documentation, and cross-functional collaboration skills. ·Fluent in English (spoken and written); additional languages are a plus.

Project title: Senior Reliability Engineer (m/w/d)
Type of employment: Payroll
Industry: Pharma
Skills: Reliability,CMMS
Project start: asap
Project duration: 31.03.2026
Location: Neuenburg, Schweiz
Home office working is acceptable but not on a full time basis


Responsibilities

  • Improve equipment and system reliability by applying reliability engineering principles in a cGMP-regulated biotech environment.
  • Analyze maintenance data to reduce downtime and optimize maintenance strategies, including preventive and predictive programs.
  • Lead root cause analyses (RCA), implement corrective/preventive actions (CAPAs), and support audit responses.
  • Define equipment importance, develop and update maintenance plans and SOPs, and ensure the effectiveness of maintenance programs.
  • Manage CMMS data, spare parts lists (BOMs/EPLs), and monitor equipment performance through trend analysis and KPIs.
  • Support capital projects, collaborate across departments (production, quality, safety, engineering), and ensure regulatory compliance (GMP, FDA).
  • Deliver training, promote reliability concepts, and maintain accurate documentation and vendor materials.
  • Drive continuous improvement initiatives for maintenance effectiveness and cost optimization.


Qualifications

  • Experience in a GMP-compliant environment with strong knowledge of operational maintenance practices.
  • Proficient in root cause analysis tools (FTA, RCA, RCFA) and data-driven decision making.
  • Working knowledge of CMMS systems such as JD Edwards or SAP.
  • Strong analytical, documentation, and cross-functional collaboration skills.
  • Fluent in English (spoken and written); additional languages are a plus.






map Neuenburg, Schweiz date_range asap update Temporary
Direkter Kontakt

Luca Furler

Senior Consultant
mail l.furler@aristo-group.ch
phone +41 44 27439 00


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