Job Details: CQV Site Manager


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
CQV Site Manager
Position: ?CQV ??Site Manager
CQV Site Manager

The CQV Site Manager reports to the Site Project Manager and CQV
Department Manager and is accountable in coordinating CQV resources,
deliverables and activities from validation approach definition,
design review, turn-over systems definition till C&Q activities at
site.

Responsibilities:

Oversight and implementation of the client CQ Program, ensuring a
quality delivery

Adherence to CQ plans for process equipment and labs scope and input
to scheduling activities

Planning, scheduling, and management of FAT attendance

Training of team members in delivery approach including KNEAT

Overview of protocol development and execution activities for Design
review, Installation Verification and

Operational Verification aspects.

Technical oversight and guidance to the CQ team.

Safety oversight of the CQ team, in collaboration with the project
safety team.

Oversight of Change Management activities during project lifecycle

Summary Report writing/ metrics / schedule reviews

Provide leadership to the C&Q teams on site

Forecast needs from various stakeholders and ensure timely
intervention to meet schedule

Driving project on schedule

Interfacing with Client representatives on project team, Engineering
Team, Quality team and End Users

during the different project phases.

Role Requirements

**Apply on the website**+ years of experience in CQV activities for
biotech pharmaceutical facilities

Strong leadership and team player ability, liaising directly with
client and other project key functions

Degree or equivalent in an engineering related discipline

Previous experience as manager/leader of C&Q team

Strong knowledge of ISPE and ASTM E**Apply on the website** Position: ?CQV ??Site Manager
CQV Site Manager

The CQV Site Manager reports to the Site Project Manager and CQV
Department Manager and is accountable in coordinating CQV resources,
deliverables and activities from validation approach definition,
design review, turn-over systems definition till C&Q activities at
site.

Responsibilities:

Oversight and implementation of the client CQ Program, ensuring a
quality delivery

Adherence to CQ plans for process equipment and labs scope and input
to scheduling activities

Planning, scheduling, and management of FAT attendance

Training of team members in delivery approach including KNEAT

Overview of protocol development and execution activities for Design
review, Installation Verification and

Operational Verification aspects.

Technical oversight and guidance to the CQ team.

Safety oversight of the CQ team, in collaboration with the project
safety team.

Oversight of Change Management activities during project lifecycle

Summary Report writing/ metrics / schedule reviews

Provide leadership to the C&Q teams on site

Forecast needs from various stakeholders and ensure timely
intervention to meet schedule

Driving project on schedule

Interfacing with Client representatives on project team, Engineering
Team, Quality team and End Users

during the different project phases.

Role Requirements

**Apply on the website**+ years of experience in CQV activities for
biotech pharmaceutical facilities

Strong leadership and team player ability, liaising directly with
client and other project key functions

Degree or equivalent in an engineering related discipline

Previous experience as manager/leader of C&Q team

Strong knowledge of ISPE and ASTM E**Apply on the website**

We need : English (Good)

Type: Permanent
Payment:
Category: Others

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