Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

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.

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 cGMP’s.
• 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 (med device or Pharma)
• 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, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html