Very likely to extend
Dublin
1 day home working
As the CSV engineer for this leading Pharmaceuticals company, you will
be responsible for leading the implementation and operation of all
automation capabilities at the new Dublin facility. The CSV engineer
must ensure that all automation activities are aligned with current
engineering standards and are executed to schedule and in accordance
with company and statutory requirements. The CSV engineer is
responsible for ensuring all automation systems are validated and
their validated status is maintained throughout the life cycle of the
system.
Duties for this role include:
Performing the role of SME for computerised/automation systems.
Owning and maintaining the site computerised system inventory.
Classifying and assessing computerised systems that support
manufacturing activities
Validating site automation systems and automation components of
equipment that support manufacturing
Managing automation-related change controls.
Acting as liaison between corporate IT and site automation.
Overseeing the validation of global computerised systems utilised on
site.
Ownership of SOPs and automation maintenance routines.
Planning and executing planned maintenance activities for automation
systems.
Maintaining of the validated state of site automation systems through
the execution of periodic reviews, security and access reviews and
automation system administration activities.
Maintaining the system risk assessments, classifications and data
integrity.Requirements:
To be considered for this role, you should have at least 6 years of
experience in Pharmaceuticals, be familiar with GAMP5 regulations,
have experience working with data integrity, and automation.
If you are interested in this role, and would like to learn more,
please respond to this advert, and I will call you to discuss in more
detail.
Please note, you must be currently based in Ireland with a valid EU
passport, or stamp 4 visa
Please click to find out more about our Key Information Documents.
Please note that the documents provided contain generic information.
If we are successful in finding you an assignment, you will receive a
Key Information Document which will be specific to the vendor set-up
you have chosen and your placement.
To find out more about Real please visit
Real Staffing, a trading division of SThree Partnership LLP is acting
as an Employment Business in relation to this vacancy| Registered
office | 1st Floor, **Apply on the website** King William Street,
London, EC4N 7BE, United Kingdom | Partnership Number | OC(phone
number removed) England and Wales **Apply on the website** month hourly rate contract
Very likely to extend
Dublin
1 day home working
As the CSV engineer for this leading Pharmaceuticals company, you will
be responsible for leading the implementation and operation of all
automation capabilities at the new Dublin facility. The CSV engineer
must ensure that all automation activities are aligned with current
engineering standards and are executed to schedule and in accordance
with company and statutory requirements. The CSV engineer is
responsible for ensuring all automation systems are validated and
their validated status is maintained throughout the life cycle of the
system.
Duties for this role include:
Performing the role of SME for computerised/automation systems.
Owning and maintaining the site computerised system inventory.
Classifying and assessing computerised systems that support
manufacturing activities
Validating site automation systems and automation components of
equipment that support manufacturing
Managing automation-related change controls.
Acting as liaison between corporate IT and site automation.
Overseeing the validation of global computerised systems utilised on
site.
Ownership of SOPs and automation maintenance routines.
Planning and executing planned maintenance activities for automation
systems.
Maintaining of the validated state of site automation systems through
the execution of periodic reviews, security and access reviews and
automation system administration activities.
Maintaining the system risk assessments, classifications and data
integrity.Requirements:
To be considered for this role, you should have at least 6 years of
experience in Pharmaceuticals, be familiar with GAMP5 regulations,
have experience working with data integrity, and automation.
If you are interested in this role, and would like to learn more,
please respond to this advert, and I will call you to discuss in more
detail.
Please note, you must be currently based in Ireland with a valid EU
passport, or stamp 4 visa
Please click to find out more about our Key Information Documents.
Please note that the documents provided contain generic information.
If we are successful in finding you an assignment, you will receive a
Key Information Document which will be specific to the vendor set-up
you have chosen and your placement.
To find out more about Real please visit
Real Staffing, a trading division of SThree Partnership LLP is acting
as an Employment Business in relation to this vacancy| Registered
office | 1st Floor, **Apply on the website** King William Street,
London, EC4N 7BE, United Kingdom | Partnership Number | OC(phone
number removed) England and Wales
We need : English (Good)
Type: Permanent
Payment:
Category: Others
