company in the Pharmaceutical industry at their site based in Swords,
Dublin on a contract basis for **Apply on the website** months.
The Company:
Our client has a long history of pushing the boundaries of science in
order to help fight some the worlds most urgent global health
challenges. This role is based at a state of the art biologics
operation where they formulate and fill vaccines and biologic
products.
The Location:
This role is located in Swords, an historic satellite town of Dublin.
Swords is located very close to Dublin airport and has excellent road
and public transport links to Dublin City and surrounding areas.
Salary:
?**Apply on the website** per hour, dependant on level of
experience.
Deviation Quality Specialist Role:
Serve as a Quality SME for site deviation management system.
Support the review and approval of site deviation and investigations
reports.
Ensure root causes have been identified and corrective action
implemented and can demonstrate basic knowledge of six sigma, LEAN,
and root cause analysis tools used for identifying and correcting
deviations.
Day to day management of Deviation and CAPA metrics.
Support internal and external audit preparations regarding deviation
management system.
Your Background:
This role requires a minimum of 3 years&#**Apply on the website**;
experience in, Quality Assurance, Technical Operations or Engineering
within the Biopharma/Pharmaceutical industry.
A self-starter and results-focussed, the successful candidate will
have strong contemporary knowledge of relevant cGMPs, regulations and
current industry trends relating to deviation investigations and CAPA
identification.
Technical experience working in regulated environment with exposure in
the Regulations & guidance&#**Apply on the website**;s - GMP, CGMP,
GAMP, **Apply on the website** CFR Part **Apply on the website**.
Must have at least 3 years of experience of deviation systems and
investigations in a regulated environment.
Must have experience of compiling and reporting QMS metrics.
Apply:
For more information or to apply for this QA Manager 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 Deviation Quality Specialist to join a
company in the Pharmaceutical industry at their site based in Swords,
Dublin on a contract basis for **Apply on the website** months.
The Company:
Our client has a long history of pushing the boundaries of science in
order to help fight some the worlds most urgent global health
challenges. This role is based at a state of the art biologics
operation where they formulate and fill vaccines and biologic
products.
The Location:
This role is located in Swords, an historic satellite town of Dublin.
Swords is located very close to Dublin airport and has excellent road
and public transport links to Dublin City and surrounding areas.
Salary:
?**Apply on the website** per hour, dependant on level of
experience.
Deviation Quality Specialist Role:
Serve as a Quality SME for site deviation management system.
Support the review and approval of site deviation and investigations
reports.
Ensure root causes have been identified and corrective action
implemented and can demonstrate basic knowledge of six sigma, LEAN,
and root cause analysis tools used for identifying and correcting
deviations.
Day to day management of Deviation and CAPA metrics.
Support internal and external audit preparations regarding deviation
management system.
Your Background:
This role requires a minimum of 3 years&#**Apply on the website**;
experience in, Quality Assurance, Technical Operations or Engineering
within the Biopharma/Pharmaceutical industry.
A self-starter and results-focussed, the successful candidate will
have strong contemporary knowledge of relevant cGMPs, regulations and
current industry trends relating to deviation investigations and CAPA
identification.
Technical experience working in regulated environment with exposure in
the Regulations & guidance&#**Apply on the website**;s - GMP, CGMP,
GAMP, **Apply on the website** CFR Part **Apply on the website**.
Must have at least 3 years of experience of deviation systems and
investigations in a regulated environment.
Must have experience of compiling and reporting QMS metrics.
Apply:
For more information or to apply for this QA Manager 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
