Pharmaceutical Documentation Specialist

1 week ago


Carlow, Ireland beBeeDocumenter Full time €55,000 - €85,000

We are seeking a highly skilled and experienced Engineer to join our team in an exciting opportunity with a leading pharmaceutical organization.

Strong documentation and GDP awareness is essential for this role. The ideal candidate will have the ability to review and follow-up technical documentation from the early design phase to ensure alignment with GMP and CQV requirements.

The successful candidate will investigate and resolve technical issues with assistance from engineers and/or suppliers, ensuring site project execution is undertaken in compliance with company guidelines, department procedures, and safety standards.

Liaising with CQV Engineers assigned to the project, the successful candidate will also manage contractors and vendors, prepare final handover reports, and coordinate with Clients PM.

To be successful in this role, you will require:

  • A minimum of 5 years post-academic experience as an E+I engineer in a relevant industry, with experience of construction & start-up.
  • Excellent communication, presentation, and organizational skills.
  • Familiarity with Fill Line and Isolator experience is desirable.
  • NQBMS and QBMS experience is also desirable.
  • Strong trouble shooting experience is essential.

This is an excellent opportunity for a motivated and organized individual to join a leading organization and contribute to its success.



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