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Decommissioning Engineer​/Biotech

Job in Cork - Ireland
Other locations:
Cork
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Company: Claran Consultants
Full Time position
Listed on 2020-09-26
Job specializations:
  • Engineering
    Electrical Engineer, Environmental Engineer, Test Engineer, Validation Engineer
  • Pharmaceutical
    Validation Engineer
Job Description & How to Apply Below
Position: Decommissioning Engineer (Biotech) - Cork county

Decommissioning Engineer required for Biotech manufacturing facility in Cork county. Will be responsible for line decommissioning. Generates of SDLC retirement plans and summary reports, executes decommissioning plans including archiving computerized control system programs and obtain SDLC packages. 11 month contract. If interested, do send an updated CV to (Please contact us using the "Apply for this Job Posting" box below)


Role
  • The Sterile IPT De-Commissioning and Validation Engineer is accountable for supporting all technical components of the process to deliver an effective and efficient facility upgrade.
  • The Sterile IPT De-Commissioning and Validation Engineer is responsible for actively participating in the Tier process to manage technical projects and proactively resolve issues before they impact the business priorities.
  • The Sterile IPT De-Commissioning and Validation Engineer will be an active member within the cross functional project team who will lead and execute all de-commissioning equipment close out activities for the assigned portion of the project.
  • The Sterile IPT De-Commissioning and Validation Engineer will participate and comply with the MMD Quality Management System (QMS) requirements and the EHS guidance chapters


Requirements
  • Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation (e.g. manufacturing, quality, engineering, etc).
  • Min 3 year’s experience in the Pharmaceutical industry or a similar operating environment with experience in a Technical role in a manufacturing environment.
  • Knowledge of and experience in De-commission and validation activities.
  • Demonstrated ability to generate, review, and execute validation protocols and reports
Position Requirements
Less than 1 Year work experience
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