Job Description:
Innovate with intention. Science is at the heart of what we do, and people are at the heart of why we do it.
Welcome to AbbVie, a global, research-based biopharmaceutical company that combines leading-edge biotech with established pharmaceutical expertise. Our mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address medical challenges tomorrow.
About Us:
We operate in key therapeutic areas - immunology, oncology, neuroscience, and eye care - and offer products and services through our Allergan Aesthetics portfolio. Our goal is to help patients live healthier lives, and we're proud to be a Great Place to Work.
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.
* Dispose of domestic, biomedical, and hazardous waste from respective areas as applicable, ensuring compliance with regulation, procedures, and policies.
* Maintain detailed records of operations carried out during the work shift.
* Test and commission equipment.
* Achieve successful external inspections and audits.
* Collaborate with Engineering, Quality, and other departments on SOP development and updates.
Requirements:
* 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, and attention to detail.