Project Engineer

  • Dublin
  • Contract 12 months
  • JO-1906-64585_1561972537

Summary

The Project engineer within the Strategic Projects group and is responsible for the scoping and execution of projects supporting Drug Product manufacturing within the Formulation, Vial/Syringe Filling, Lyophilisation, Inspection, Component Preparation and Packaging areas. This includes implementation of maintenance programs associated with the introduction of new equipment.

Key Responsibilities

* Project management and execution of assigned projects including project prioritization, resources management, status management and external communication.

* Working with various stakeholders, to scope the project and ensure the requirements are satisfied. Project input will span from concept, through design and on to construction, commissioning and operation

* Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues during start-up and qualification.

* Development and implementation of maintenance programs associated and spare parts inventory optimization with the introduction of new equipment.

* Ability to translate strategic opportunities and emerging technology solutions into tangible pragmatic executable plans

* Development and management of change controls

* Participate as a member of multidisciplinary site and multisite teams

* Development of detailed specifications, engineering documents, protocols and standard operating procedures

* Works in a collaborative manner within the Process Teams structure and contributes to investigations, Cross Functional Investigations etc.

* Works in a collaborative manner with the System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits.

* Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures

* Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations

Requirements:

* Bachelors degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience

* Typically 4+ years engineering experience, preferably in the biotechnology/bio-processing industry

* Demonstrated experience in a GDP Compliant environment.

* Experience in MS Office, MS Project, Change Control & Document Management Systems

* Proven ability around working cross functionally, delivering technical solutions and identifying improvements.

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