Validation Engineer

Occupli

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profile Job Location:

Dundalk - Ireland

profile Monthly Salary: Not Disclosed
profile Experience Required: 5years
Posted on: 9 hours ago
Vacancies: 1 Vacancy

Job Summary


Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.

This role will play a critical part in delivering validation activities across key projects with a strong focus on equipment performance qualification including cleaning and sterilisation processes.

Key Responsibilities:

  • Lead planning and execution of Equipment/Engineering Performance Qualification (EMPQ) activities

  • Develop Validation Master Plans and associated validation lifecycle documentation

  • Author and execute validation protocols and comprehensive summary reports

  • Analyse validation data and provide clear technical conclusions

  • Update and improve SOPs and validation documentation as required

  • Troubleshoot and resolve technical challenges during study execution

  • Collaborate effectively within cross-functional project teams while also operating independently





Requirements


  • Proven experience in EMPQ planning and execution within a regulated pharmaceutical manufacturing environment

  • Strong technical writing skills with a high level of documentation accuracy

  • Ability to work with minimal supervision and drive deliverables to completion

  • Confident communicator with strong problem-solving capability


Benefits

This is an excellent opportunity for a validation professional who thrives in a dynamic compliance-driven manufacturing environment and can deliver high-quality results with limited oversight.




Required Skills:

5 years experience in EHS within pharmaceutical biotech medical device chemical or other manufacturing environments. Developing knowledge of Construction Safety Process Safety and regulatory compliance. Ability to conduct basic risk assessments and support EHS documentation and reporting. Strong communication teamwork and problem-solving abilities.


Required Education:

Degree in Environmental Chemical Safety Engineering or a related technical field

Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.This role will play a critical part in delivering validation activities across key projects with a strong focus on equipment pe...
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Company Industry

IT Services and IT Consulting

Key Skills

  • Python
  • SOC
  • Debugging
  • C/C++
  • FDA Regulations
  • Minitab
  • Technical Writing
  • GAMP
  • OS Kernels
  • Perl
  • cGMP
  • Manufacturing