experience in commissioning and qualification activities for
pharmaceutical facilities and have previous experience as
manager/leader of C&Q team?
If you have the relevant experience, please forward your CV to **Apply
on the website** for review or call * **Apply
on the website** to discuss in confidence.
SENIOR CQV ENGINEER FOR CLEAN UTILITIES – EXECUTION PHASE -
PHARMA- IRELAND
JOB DESCRIPTION
Our client is an international engineering and PM consultancy with
Life Science projects across Ireland.
Manage team of C&Q Engineers on high profile client site throughout
the project lifecycle.
Strong experience with Validation Master Plan, Commissioning Master
Plan, project procedures and commissioning and qualification protocols
(SAT/Commissioning, IQ and OQ)
Design Review (DR) process and GMP Risk Assessment (FMEA) experience
Identify the appropriate Commissioning and Qualification strategy to
apply on specific project and define the list of activities required
Review and follow-up technical documentation from the early design
phase in order to ensure alignment with GMP and CQV requirements
Investigate and resolve technical issues with assistance from Jacobs
engineers and/or suppliers
Ensure site project execution is undertaken in compliance with company
guideline, department procedures and safety standards
Be familiar with the Mechanical Completion procedure and Construction
scope of work (Walkdown, system acceptance, punch list and follow up)
Schedule preparation and progress review
Organize and review daily activities of other CQV Engineers assigned
to the project
Project management principles to coordinate CQV activities and
reporting to Jacobs and Clients PM
Contractors and Vendors management and coordination
Final Handover reports to the Client users
The Senior CQV Engineer reports to the department manager / site
commissioning manager and is accountable to coordinate CQV resources,
deliverables and activities from the validation approach definition,
design review, turn-over systems definition and C&Q activities at
site.
REQUIREMENTS
Degree or equivalent in an engineering related discipline
*+ years of experience in commissioning and
qualification activities for pharmaceutical facilities
Strong leadership and team player ability, liaising directly with
client and other project key functions
Previous experience as manager/leader of C&Q team
Strong knowledge of ISPE and ASTM E *
Proven experience with international pharmaceutical projects
Mentor for junior staff members
PACKAGE
Competitive hourly rate of € * - €**Apply on
the website** per hour
Minimum Contract of * months
Hybrid Working
We need : English (Good)
Type: Permanent
Payment: EUR 65 - 75 Per Hour
Category: Construction
