commissioning in pharma / biotech / API?
If interested in this role, call Karen on +**Apply on the
website**- * to discuss or forward your CV to
* for review
CQV ENGINEER - PHARMA - TIPPERARY
JOB DESCRIPTION
Our client is an international engineering and PM consultancy with
Life Science projects across Ireland.
The C&Q Engineer shall be responsible for carrying out the following
project related activities:
Preparation of documents associated with lifecycle of C&Q activities
for a IV, FT, IQ, OQ.
Preparation and execution of FAT, Commissioning and SAT protocols
Preparation and execution of Qualification protocols (IQ and OQ)
Design Review (DR) and Design Qualification (DQ) protocol preparation,
execution and follow-up
Field Walkdowns of systems as part of transfer of ownership of the
system from Construction
Ensuring safe operation of the system prior to and during start-up
functional testing and Qualification phases
Installation Verification execution
System Startup activities
Functional Testing of systems
Change Management activities during project lifecycle
Summary Report writing
Organize and review daily tasks/verifications and track the progress
of the activities assigned
Contractors and/or Vendors coordination
Interfacing with representatives on project team, Construction,
Engineering, Automation, Quality and End Users during the different
project phases
REQUIREMENTS
A degree in science or engineering or equivalent.
4+ years experience of field commissioning in pharma / biotech / API
Experience with Regulatory and industry standards for GMP and GEP
Self starter & good team player
Good oral & written communication skills
PACKAGE
Contract hourly rate € * - €**Apply on the
website** per hour
We need : English (Good)
Type: Permanent
Payment: EUR 65 - 75 Per Hour
Category: Construction
