Project Engineer

3 weeks ago

Dublin, Dublin City, Ireland Ascend Project Management Full time
Overview

The Project / Equipment Engineer reports to the Senior Manager for Strategic Engineering Projects and is responsible for scoping and executing technical projects supporting Drug Product manufacturing within Formulation, Component Preparation, Vial/Syringe Filling, Lyophilisation, Device Assembly, Inspection, Filter/Filter Integrity Testing areas. This includes qualification of new equipment and implementation of associated reliability and maintenance programs. This is a 12 Month Contract opportunity with potential to extend. Contact or email CV to clairebrogan@ascendpm.ie to find out more.

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 projects and ensure requirements are satisfied. Project input will span from concept, through design, construction, commissioning and operation.
  • Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification & start-up.
  • Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment.
  • Ability to translate strategic/emerging technology solutions into 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.
  • Work in a collaborative manner within the Process Teams structure and contribute to Root Cause Investigations and Cross Functional Investigations.
  • Work with System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers and Vendors to perform equipment upgrades 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 environmental health/safety practices, rules and regulations.
  • Travel may be required to support execution of projects.
Experience and Qualifications
  • Bachelor's Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience.
  • Typically, 3+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection and/or Automated Device Assembly.
  • Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous.
  • Demonstrated experience in a GDP Compliant environment.
  • Experience in MS Office, MS Project, Change Control & Document Management Systems.
  • Proven ability working cross functionally, delivering technical solutions and implementing improvements.
  • Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results.
  • Technical report writing and communication/presentation skills.
Seniority level
  • Mid-Senior level
Employment type
  • Contract
Industries
  • Pharmaceutical Manufacturing

Notes: The listing originally included multiple unrelated postings and timestamps from the job board. This refined version retains the core job information and removes extraneous content.


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