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

WHAT YOU WILL NEED:

• 3rd level qualification in a relevant Science discipline
• 4+ years experience in a Biologics position
• Antibody drug, ADC and drug substance purification experience preferable
  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 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.htm

• You will be assigned to the daily production operations, operating different equipment.
• Efficiently operate all biologics processes minimizing material loss.
• Documentation of all activities in line with cGMP requirements.
• Perform final product visual inspection.
• Perform product intermediary packaging, as applicable.
• Perform all in process testing methods.
• Material receipt from warehouse, verifying all pertinent documentation.
• Transfer of final material to warehouse inventory.
• Perform process tests and participate in qualification and validation activities as required.
• 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.
• Adhering to all relevant policies relating to Quality & Safety.
• Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures