Manufacturing Shift Engineer

Vetamc

Dunboyne, County Meath, Ireland
Onsite
Process engineering systems
Real-time process monitoring
Troubleshooting
Vetamc is seeking a Manufacturing Shift Engineer for their new biotech facility in Dunboyne, Ireland. The role involves providing technical support, optimizing processes, and ensuring compliance in a regulated manufacturing environment

Job Summary

  • The Shift Engineer will work across the site teams to identify and resolve issues in order to allow the site to deliver on our commitment to support Quality, EHS, Technical problem solving and Continuous improvement.
  • The role will involve being a key point of contact and liaison between Manufacturing Operations and Manufacturing Technical Support, working as part of a team of scientists, engineers and support specialists who will be responsible for supporting routine batch activities and transform the business initiatives.
  • Responsible for the generation and approval of GMP documentation to support compliance and regulatory expectations for manufacturing operations: change control management and implementation, closure of significant technical investigations, process improvement opportunity identification through implementation, regulatory license section authoring through response-to questions, health authority inspection SME support, and more.

Matching Summary

Match Score: 85

Vetamc is seeking a Manufacturing Shift Engineer for their new biotech facility in Dunboyne, Ireland. The role involves providing technical support, optimizing processes, and ensuring compliance in a regulated manufacturing environment.

Skills & Requirements

Must-have

  • Process Engineering Systems
  • Real-time process monitoring
  • Troubleshooting
  • Risk management techniques
  • cGMP Guidelines
  • Electronic Batch Records
  • Manufacturing Engineering

Nice-to-have

  • Continuous improvement methodologies
  • Collaboration, negotiation, conflict resolution
  • Interfacing with regulators
  • Lean QA
  • 5S

Key Requirements

  • Minimum Level 8 qualification
  • 3-5 years experience
  • Regulated pharmaceutical manufacturing environment
  • Global regulatory experience

Work Rights

Not specified

Tailored Resume

Cover Letter