Project Engineer

Contract: 24 months (initial 12-month)
Apply below after reading through all the details and supporting information regarding this job opportunity.

Location: Eastern & Midland Region, Ireland (on-site)

Serve as Occupli’s client-representative within the Global Engineering Team,providing project engineering support for commissioning and qualification of adrug substance / drug product manufacturing facility. You will help managecross-functional teams to deliver key C&Q milestones.

• 
  
• Developand maintain project schedules, work plans, and cost-tracking forequipment and capital.
  
• Coordinateacross stakeholders including engineering, validation, quality,operations, and vendors.
  
• Leadinstallation, start-up, and testing through Operational Qualification(OQ).
  
• Supportreadiness for post-OQ phases (PQ, PPQ), ensuring design and validationdeliverables reflect site and business requirements.
  
• Monitorproject progress, costs, and risks; produce tiered status reporting.
  
• Engagewith cross-functional experts, SMEs, and vendor partners to ensurealignment.
  
• Assistin regulatory and validation documentation, including CAPAs and riskassessments.
  
• Drivecontinuous improvement in C&Q execution and handover processes.
  

• 
  
• Bachelor’sor Master’s degree in Engineering (Mechanical, Process, Chemical, etc.).
  
• Minimum6 years’ experience in a commissioning / qualification / validation role —ideally in a sterile or aseptic manufacturing environment.
  
• Experiencewriting and executing IQ/OQ (and preferably PQ) protocols.
  
• Strongproject coordination, communication and stakeholder engagement skills.
  
• Demonstratedability to collaborate cross-functionally and work as part of a team.
  

• 
  
• Knowledgeof GMP, risk-based validation (e.g. FMEA), and ISPE / GAMP frameworks.
  
• Experiencewith FAT / SAT, vendor management, and commissioning change control.
  

• 
  
• Workon a high-impact project in a leading pharmaceutical manufacturingfacility.
  
• Bepart of an international engineering team and contribute tocritical qualification phases.
  
• Gain contract-based flexibility with the opportunity to make ameasurable difference. xcfaprz
  
• Opportunityto deepen your expertise in pharma commissioning & validation.