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Operations Process Support Specialist

  1. East
Carlow
  1. Contract
Competitive
  1. CAPEX Projects
34479

This vacancy has now expired

Operations Process Support Specialist – Contract – Ireland

With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for an Operations Process Support Specialist to join their team to support multiple capital projects taking place onsite in Carlow.

This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:
  • Serve as a technical and operations representative for established manufacturing processes and new product introduction.
  • Collaborate within cross-functional teams and partner with colleagues to perform vendor management, communications, training, project work, audit/inspection duties, and ensure department readiness for audits/inspections.
  • Design, author, review, approve, and execute process updates in support of ongoing manufacturing support and new product introduction.
  • Provide technical input into quality notifications by authoring, reviewing, and approving investigations.
  • Drive continuous process improvements using Lean Principles to optimise equipment uptime and target outputs.
  • Oversee operations processes to ensure continuous, reliable, and repeatable manufacturing.
  • Drive effective writing, revising, and rolling out of accurate operational procedures, training materials, and manufacturing procedures.
Requirements:
  • Bachelor’s Degree or equivalent, ideally in a Science, Engineering or other Technical discipline
  • Proven track record and established experience in a process engineer role with measurable accomplishments and achievements.
  • Relevant experience and a particular skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably in a GMP setting.
  • Knowledge of regulatory and code requirements to Irish, European, and International Codes, Standards, and Practices.
  • Proficiency in report, standards, and policy writing.
If you are interested initially, please apply now for immediate consideration and further information.
 #LI-JS5
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