biopharmaceutical company at their site based in Innishannon on a on a
contract basis for **Apply on the website** months.
Company:
Our client is a global health care leader with a diversified portfolio
of prescription medicines, vaccines and animal health products. They
have an interdependent global manufacturing network that&#**Apply on
the website**;s committed to delivering a compliant, reliable supply
to customers and patients on time, every time, across the globe.
Location:
This QA IT Specialist role will be based at our clients manufacturing
site in Innishannon, County Cork.
Salary:
From ?**Apply on the website** per hour depending upon experience.
QA IT Specialist Role:
Providing independent quality review and approval of system lifecycle
documentation, such as plans, requirements, risk assessments, test
protocols and reports for new and modified systems.
Providing independent quality review and approval of system changes.
Supporting and approving computerised systems investigations and
deviations.
Ensuring consistent approach to qualification, change and deviation
management across systems and projects.
Managing and prioritising day-to-day activities through active
alignment with the project team, and supporting other areas as needed.
Your Background:
Min. 5 years of experience in QA IT/CSV, CSV and/or a similar role in
the pharmaceutical industry.
Expert knowledge of relevant regulations and industry standards.
Project management experience will be an advantage.
PLC/SCADA, OSI PI and PAS-X experience will be an advantage.
Apply:
For more information or to apply for this QA IT Specialist position,
please contact Natasha on (phone number removed) or email (url
removed), quoting job ref **Apply on the website**.
It is essential that applicants hold entitlement to work in Ireland CK Group are recruiting for a QA IT Specialist to join a
biopharmaceutical company at their site based in Innishannon on a on a
contract basis for **Apply on the website** months.
Company:
Our client is a global health care leader with a diversified portfolio
of prescription medicines, vaccines and animal health products. They
have an interdependent global manufacturing network that&#**Apply on
the website**;s committed to delivering a compliant, reliable supply
to customers and patients on time, every time, across the globe.
Location:
This QA IT Specialist role will be based at our clients manufacturing
site in Innishannon, County Cork.
Salary:
From ?**Apply on the website** per hour depending upon experience.
QA IT Specialist Role:
Providing independent quality review and approval of system lifecycle
documentation, such as plans, requirements, risk assessments, test
protocols and reports for new and modified systems.
Providing independent quality review and approval of system changes.
Supporting and approving computerised systems investigations and
deviations.
Ensuring consistent approach to qualification, change and deviation
management across systems and projects.
Managing and prioritising day-to-day activities through active
alignment with the project team, and supporting other areas as needed.
Your Background:
Min. 5 years of experience in QA IT/CSV, CSV and/or a similar role in
the pharmaceutical industry.
Expert knowledge of relevant regulations and industry standards.
Project management experience will be an advantage.
PLC/SCADA, OSI PI and PAS-X experience will be an advantage.
Apply:
For more information or to apply for this QA IT Specialist position,
please contact Natasha on (phone number removed) or email (url
removed), quoting job ref **Apply on the website**.
It is essential that applicants hold entitlement to work in Ireland
We need : English (Good)
Type: Permanent
Payment:
Category: Others
