Manufacturing Visual Inspection Technician

AbbVie

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profile Job Location:

Sligo - Ireland

profile Monthly Salary: Not Disclosed
Posted on: 8 hours 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 Manufacturing Visual Inspection Technician to join a brand new team on our site in Ballytivnan Sligo. You will work as a team member to support biologics operations in pharma operations in line with all safety regulatory and organizational requirements.

This role will require shift work.

Are you intrigued Do you want to learn more

Responsibilities:

  • Document all activities in line with cGMP requirements.
  • Perform final product visual inspection.
  • Perform product intermediary packaging as applicable.
  • Perform process testing methods.
  • Monitor Process Alarms.
  • Transfer final materials to warehouse inventory.
  • Ensure all manufacturing documentation is completed in a timely manner without errors following cGMPs.
  • Diagnose and resolve events or exceptions of VI process.
  • Disposal of domestic biomedical and hazardous waste from their respective area as applicable ensuring compliance with regulation 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.
  • 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.
  • Work with Engineering Quality and other departments in the development and update of Standard Operating Procedures.

Qualifications :

What you will need: 

  • 3rd level qualification in a relevant Science discipline OR 2 years of experience in a GMP Environment
  • Previous experience in a GMP environment (Pharma preferably)
  • Flexibility great concentration & attention to detail

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 :

No


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...
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About Company

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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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