Quanta are currently supporting a bio-pharma client based in Dublin
with a small facility expansion project. The client is looking for a
CQV Manager who would be able to support them with CQV strategy and
lead all CQV activities from early design stages through to project
completion. The successful CQV Manager will be responsible for:
Creating the CQV strategy and supporting its execution
Supporting the commissioning, qualification and validation of
equipment.
Reviewing vendor documents to support commissioning and qualification
requirements.
Completing the development, review, and execution of validation plans,
URSs/DQ/FATs/SATs/IQ/OQ protocols/reports.
Ensures validation non-conformances or deviations are minimised during
execution of CQV activities.
Coordinates with other departments or outside contractors/vendors to
complete validation tasks.
Provide knowledge and expertise to wider Project team and work closely
with other Departments.
Other duties as required and directed by the Project Director.
Experience required:
This individual should have worked as part of a project supporting the
full life-cycle of activities.
Previous experience in Senior Engineer/Lead positions on similar
projects.
Knowledge of validation practices and regulatory guidelines for a
bio-pharma / pharmaceutical facility.
Experience in a GMP environment essential.
If this sound like you or anybody in your network, please get in
touch!
The candidate must have the rights to work in the location stated in
the job advert. Please note, Quanta part of QCS Staffing does not
sponsor Visa applications.
To view Quanta&#**Apply on the website**;s privacy policy, please CQV Manager ? Contract ? Bio-pharma Expansion Project - ASAP
Quanta are currently supporting a bio-pharma client based in Dublin
with a small facility expansion project. The client is looking for a
CQV Manager who would be able to support them with CQV strategy and
lead all CQV activities from early design stages through to project
completion. The successful CQV Manager will be responsible for:
Creating the CQV strategy and supporting its execution
Supporting the commissioning, qualification and validation of
equipment.
Reviewing vendor documents to support commissioning and qualification
requirements.
Completing the development, review, and execution of validation plans,
URSs/DQ/FATs/SATs/IQ/OQ protocols/reports.
Ensures validation non-conformances or deviations are minimised during
execution of CQV activities.
Coordinates with other departments or outside contractors/vendors to
complete validation tasks.
Provide knowledge and expertise to wider Project team and work closely
with other Departments.
Other duties as required and directed by the Project Director.
Experience required:
This individual should have worked as part of a project supporting the
full life-cycle of activities.
Previous experience in Senior Engineer/Lead positions on similar
projects.
Knowledge of validation practices and regulatory guidelines for a
bio-pharma / pharmaceutical facility.
Experience in a GMP environment essential.
If this sound like you or anybody in your network, please get in
touch!
The candidate must have the rights to work in the location stated in
the job advert. Please note, Quanta part of QCS Staffing does not
sponsor Visa applications.
To view Quanta&#**Apply on the website**;s privacy policy, please
We need : English (Good)
Type: Permanent
Payment:
Category: Others
