Pharmaceutical Commissioning Expert

1 week ago

Cork, Cork, Ireland beBeeCqvsiteengineer Full time €90,000 - €120,000
CQV Site Engineer Job Opportunity

We are seeking an experienced CQV Site Engineer to join our team on a Pharmaceutical project.

Key Responsibilities:
  • Manage a team of commissioning and qualification engineers throughout the project lifecycle.
  • Develop validation master plans, commissioning master plans, and project procedures.
  • Design review process and GMP risk assessment.
  • Identify commissioning and qualification strategy and define required activities.
  • Audit technical documentation for alignment with GMP and CQV requirements.
  • Coordinate CQV activities and reporting.
  • Contractor and vendor management.
  • Final handover reports to client users.
Required Skills and Qualifications:
  • 10+ years of experience in commissioning and qualification activities for pharmaceutical facilities.
  • Degree or equivalent in an engineering-related discipline.
  • Proven experience as manager/leader of a C&Q team.
  • Excellent leadership and team player skills.
  • Strong knowledge of ISPE and ASTM E2500 standards.
  • Experience with international pharmaceutical projects.
  • Mentoring junior staff members.
Benefits:

This is a 14-month contract position offering a hybrid work arrangement based in Co. Tipperary.

We offer a competitive compensation package that includes salary, benefits, and opportunities for career growth and development.

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