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