Location: Not Specified
QA Validation Consultant - Change Control
We are helping the leading biotechnology company to find the best QA
Validation Consultant to join their fantastic team in Limerick!!
This is a **Apply on the website**-month contract and an excellent
opportunity to get into a very secure company during this difficult
time.
The successful candidate will be coordinating and maintaining the site
Change Control process to ensure that this key element of the Quality
Management System continuously operates in a compliant manner while
meeting ongoing business requirements.
The role may also involve supporting other quality system elements
such as Deviations, CAPA or QRM as required.
Essential Duties and Responsibilities include, but are not limited to,
the following:
Responsible for ensuring compliance with all aspects of Quality for
the Limerick site inclusive of manufacturing, quality systems, quality
control, validation, facilities, and materials management.
Primarily responsible for administration and oversight of the Change
Control process but may also be responsible for one or more of the
site quality systems including but not limited to;
* Deviations
* CAPA
* Quality Risk Management
* Responsible for review and approval of associated change control
documents, and other documents such as:
* Failure investigations
* corrective/preventative action documents
* Standard operating procedures
* Maintaining the electronic systems used for Change Control,
Deviation Management and CAPA.
* Reviews procedures, policies and other instructional documents
relating to quality systems to ensure compliance with company policy
and local and international regulatory requirements
* Provision of monitoring and trending metrics associated with change
control and other site quality systems
* Actively participate in continuous improvement initiatives.
* Participates in regulatory and customer audits.
* Participates in quality risk assessments.
* Collaborates with functional departments to resolve issues and
maintain compliance
* Identify gaps in systems and develop feasible plans for correction
* Training of personnel on change control and other quality system
processes
If you would like to learn more, send an email to ring on (phone
number removed) or apply.
Clicking the "Apply Now" button means that you agree to the processing
of your personal data for the purposes of current and future
recruitment processes, carried out by QPTech in accordance with the
provisions of the General Data Protection Regulation (GDPR) (EU)
**Apply on the website**/**Apply on the website**. You also agree to
share your personal data with other entities of QPTech and potential
employers for purposes related to the recruitment process. QPTech may
also contact you from time to time to inform you of events we are
hosting that you may find interesting.
Providing data is voluntary, you have the right to inspect, correct or
request deletion of your data at any time. A request to delete data
means withdrawal from any further engagement in QPTech&#**Apply on the
website**;s recruitment processes and will result in the immediate
deletion of your data. If you do not agree, please do not click the
"Apply Now" button.
Please visit QPTech&#**Apply on the website**;s website to read the
full Privacy Policy (https(url removed) Position: QA Validation Consultant - Limerick
Location: Not Specified
QA Validation Consultant - Change Control
We are helping the leading biotechnology company to find the best QA
Validation Consultant to join their fantastic team in Limerick!!
This is a **Apply on the website**-month contract and an excellent
opportunity to get into a very secure company during this difficult
time.
The successful candidate will be coordinating and maintaining the site
Change Control process to ensure that this key element of the Quality
Management System continuously operates in a compliant manner while
meeting ongoing business requirements.
The role may also involve supporting other quality system elements
such as Deviations, CAPA or QRM as required.
Essential Duties and Responsibilities include, but are not limited to,
the following:
Responsible for ensuring compliance with all aspects of Quality for
the Limerick site inclusive of manufacturing, quality systems, quality
control, validation, facilities, and materials management.
Primarily responsible for administration and oversight of the Change
Control process but may also be responsible for one or more of the
site quality systems including but not limited to;
* Deviations
* CAPA
* Quality Risk Management
* Responsible for review and approval of associated change control
documents, and other documents such as:
* Failure investigations
* corrective/preventative action documents
* Standard operating procedures
* Maintaining the electronic systems used for Change Control,
Deviation Management and CAPA.
* Reviews procedures, policies and other instructional documents
relating to quality systems to ensure compliance with company policy
and local and international regulatory requirements
* Provision of monitoring and trending metrics associated with change
control and other site quality systems
* Actively participate in continuous improvement initiatives.
* Participates in regulatory and customer audits.
* Participates in quality risk assessments.
* Collaborates with functional departments to resolve issues and
maintain compliance
* Identify gaps in systems and develop feasible plans for correction
* Training of personnel on change control and other quality system
processes
If you would like to learn more, send an email to ring on (phone
number removed) or apply.
Clicking the "Apply Now" button means that you agree to the processing
of your personal data for the purposes of current and future
recruitment processes, carried out by QPTech in accordance with the
provisions of the General Data Protection Regulation (GDPR) (EU)
**Apply on the website**/**Apply on the website**. You also agree to
share your personal data with other entities of QPTech and potential
employers for purposes related to the recruitment process. QPTech may
also contact you from time to time to inform you of events we are
hosting that you may find interesting.
Providing data is voluntary, you have the right to inspect, correct or
request deletion of your data at any time. A request to delete data
means withdrawal from any further engagement in QPTech&#**Apply on the
website**;s recruitment processes and will result in the immediate
deletion of your data. If you do not agree, please do not click the
"Apply Now" button.
Please visit QPTech&#**Apply on the website**;s website to read the
full Privacy Policy (https(url removed)
We need : English (Good)
Type: Permanent
Payment:
Category: Others
