Headcount Engineering is seeking 3 Project Engineers for an expansion
project at our client&#**Apply on the website**;s biotech facility.
These candidates will be required to work closely with a
cross-functional team and coordinate activities between Design,
Construction, Process, Technical Operations, C&Q, IPT and QA.
They will provide process engineering services in support of the
design, construction, commissioning and qualification of a Sterile
Formulation and Filling Facility.
Responsibilities:
* Assist in the development and delivery, within the overall project
schedule, of a schedule for the delivery of all aspects of the Suite
scope.
* Develop, document, agree and implement an execution strategy to
deliver the scope in a controlled and well communicated manner.
* Monitor progress of process suite team milestones with all team
members and provide status reports to project Tiers and stakeholders.
* Develop and/or review system lifecycle documents including
Criticality and Risk assessments, FAT documentation, and C&Q
documentation.
* Support installation / start-up / testing of process systems through
OQ completion. Interface with cross-functional team to ensure
systems&#**Apply on the website**; post-OQ (PQ, PPQ) readiness.
* Provide coordination expertise during C&Q activities as needed.
* Assist in the coordinating of C&Q start-up activities, punch list
follow-up.
* Facilitate/expedite Mechanical Completion in conjunction with the
Construction team. (Liaise with construction contractors towards
successful completion of Construction Turn Over Documentation).
* Delivery of the agreed milestones on the schedule within budget
constraints.
* Delivery of stakeholder agreed scope for Suite facilities to
Commissioning Qualification or as appropriate Process Qualifications.
Requirements:
* Bachelor of Engineering or Science Degree in Engineering or
Technology related discipline.
* Minimum of 6 years&#**Apply on the website**; experience similar
role in Pharmaceutical Facility/ Building/Utilities systems within
Pharmaceutical industry.
* Working knowledge of standards as they apply in biotechnology
processes industries and a working knowledge of FDA and EU regulations
is preferred.
* Experience of design and construction/handover of pharmaceutical
process and building facilities for pharmaceutical facilities.
* Ability to work in design and construction large project environment
within Ireland.
* The candidate will be a convincing communicator with strong
interpersonal skills
* Working knowledge of control systems and automation.
* Working knowledge of C&Q documentation required for cGMP project
delivery.
For further information please contact Mick on (phone number removed)
or forward details in confidence to Projects Engineers
Headcount Engineering is seeking 3 Project Engineers for an expansion
project at our client&#**Apply on the website**;s biotech facility.
These candidates will be required to work closely with a
cross-functional team and coordinate activities between Design,
Construction, Process, Technical Operations, C&Q, IPT and QA.
They will provide process engineering services in support of the
design, construction, commissioning and qualification of a Sterile
Formulation and Filling Facility.
Responsibilities:
* Assist in the development and delivery, within the overall project
schedule, of a schedule for the delivery of all aspects of the Suite
scope.
* Develop, document, agree and implement an execution strategy to
deliver the scope in a controlled and well communicated manner.
* Monitor progress of process suite team milestones with all team
members and provide status reports to project Tiers and stakeholders.
* Develop and/or review system lifecycle documents including
Criticality and Risk assessments, FAT documentation, and C&Q
documentation.
* Support installation / start-up / testing of process systems through
OQ completion. Interface with cross-functional team to ensure
systems&#**Apply on the website**; post-OQ (PQ, PPQ) readiness.
* Provide coordination expertise during C&Q activities as needed.
* Assist in the coordinating of C&Q start-up activities, punch list
follow-up.
* Facilitate/expedite Mechanical Completion in conjunction with the
Construction team. (Liaise with construction contractors towards
successful completion of Construction Turn Over Documentation).
* Delivery of the agreed milestones on the schedule within budget
constraints.
* Delivery of stakeholder agreed scope for Suite facilities to
Commissioning Qualification or as appropriate Process Qualifications.
Requirements:
* Bachelor of Engineering or Science Degree in Engineering or
Technology related discipline.
* Minimum of 6 years&#**Apply on the website**; experience similar
role in Pharmaceutical Facility/ Building/Utilities systems within
Pharmaceutical industry.
* Working knowledge of standards as they apply in biotechnology
processes industries and a working knowledge of FDA and EU regulations
is preferred.
* Experience of design and construction/handover of pharmaceutical
process and building facilities for pharmaceutical facilities.
* Ability to work in design and construction large project environment
within Ireland.
* The candidate will be a convincing communicator with strong
interpersonal skills
* Working knowledge of control systems and automation.
* Working knowledge of C&Q documentation required for cGMP project
delivery.
For further information please contact Mick on (phone number removed)
or forward details in confidence to
We need : English (Good)
Type: Permanent
Payment:
Category: Others
