Senior MVI Technician

Sligo - Ireland

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Innovate with intention.

Science is at the heart of what we do. People are at the heart of why we do it.

Welcome to AbbVie!

We are a global research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.

We are recruiting a Senior MVI Technician to join our site in Ballytivnan Sligo. This role will require shift work.

Are you intrigued Do you want to learn more

A snapshot of your key responsibilities as a Senior MVI Technician would be:

To work as a team member to support biologics operations in line with all safety regulatory and organizational requirements.
Provide support on change controls investigations tasks and CAPAs for the Biologics Operations Department.
To support the Operations Lead in line with safety regulatory and organisational requirements when delegated responsibility.
Co-ordination between shift teams to ensure excellence in GMP/ safety and manufacturing activities
Point of Contact for Manufacturing issues which arise and if escalation to Supervisor is required.
Efficiently operate all biologics processes minimizing material loss.
Operate Fill Line Autoclave Equipment Washer Headspace Analyzer Filtration Systems Equipment Cleaning and Sterilization Equipment Pressure Tests Equipment/Filters Integrity Tests Water Baths Isolators and Lyophiliser as applicable.
Perform Operations Batch Review as Required
Perform final product visual inspection as required
Perform product intermediary packaging as applicable.
Assemble and inspect equipment in the manufacturing area to confirm its operational status.
Perform all in process testing methods.
Material receipt from warehouse verifying all pertinent documentation & completion of all relevant transactions on SAP/POMS
Completion of Inventory Counts as required
Transfer of final material to warehouse inventory.
Perform process tests and participate in qualification and validation activities as required.
Ensure all manufacturing documentation is completed on a timely manner without errors following cGMPs
Diagnose and resolve events or exceptions of production equipment and processes.
Disposal of domestic biomedical and hazardous waste from their respective area as applicable ensuring compliance with regulations following the procedures and policies of the plant division and the corporation.
Keep detailed records manual or electronic of the operations carried out during the work shift.
Active Participation in Factory Acceptance testing Site Acceptance Testing and commissioning and qualification of equipment.
Adhering to all relevant policies relating to Quality & Safety.
Ensure successful external inspections and Division and Corporate audits.
Active participant in the development of batch records and electronic batch records for the site & primary reviewer for the batch records in development.

Qualifications :

What you will need:

3rd level qualification in a relevant Science discipline
3 years experience in a similar position

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Innovate with intention.Science is at the heart of what we do. People are at the heart of why we do it.Welcome to AbbVie!We are a global research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceut...

Innovate with intention.

Science is at the heart of what we do. People are at the heart of why we do it.

Welcome to AbbVie!

We are recruiting a Senior MVI Technician to join our site in Ballytivnan Sligo. This role will require shift work.

Are you intrigued Do you want to learn more

A snapshot of your key responsibilities as a Senior MVI Technician would be:

To work as a team member to support biologics operations in line with all safety regulatory and organizational requirements.
Provide support on change controls investigations tasks and CAPAs for the Biologics Operations Department.
To support the Operations Lead in line with safety regulatory and organisational requirements when delegated responsibility.
Co-ordination between shift teams to ensure excellence in GMP/ safety and manufacturing activities
Point of Contact for Manufacturing issues which arise and if escalation to Supervisor is required.
Efficiently operate all biologics processes minimizing material loss.
Operate Fill Line Autoclave Equipment Washer Headspace Analyzer Filtration Systems Equipment Cleaning and Sterilization Equipment Pressure Tests Equipment/Filters Integrity Tests Water Baths Isolators and Lyophiliser as applicable.
Perform Operations Batch Review as Required
Perform final product visual inspection as required
Perform product intermediary packaging as applicable.
Assemble and inspect equipment in the manufacturing area to confirm its operational status.
Perform all in process testing methods.
Material receipt from warehouse verifying all pertinent documentation & completion of all relevant transactions on SAP/POMS
Completion of Inventory Counts as required
Transfer of final material to warehouse inventory.
Perform process tests and participate in qualification and validation activities as required.
Ensure all manufacturing documentation is completed on a timely manner without errors following cGMPs
Diagnose and resolve events or exceptions of production equipment and processes.
Disposal of domestic biomedical and hazardous waste from their respective area as applicable ensuring compliance with regulations following the procedures and policies of the plant division and the corporation.
Keep detailed records manual or electronic of the operations carried out during the work shift.
Active Participation in Factory Acceptance testing Site Acceptance Testing and commissioning and qualification of equipment.
Adhering to all relevant policies relating to Quality & Safety.
Ensure successful external inspections and Division and Corporate audits.
Active participant in the development of batch records and electronic batch records for the site & primary reviewer for the batch records in development.

Qualifications :

What you will need:

3rd level qualification in a relevant Science discipline
3 years experience in a similar position

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Key Skills

Computer Operation
Computer Skills
Generator Repair
Military Experience
Mechanical Knowledge
Commercial Driving
HVAC/R
Ftp
Schematics
Maintenance
Medical Imaging
Troubleshooting

Apply Now

About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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