Scientist, II - Global Material and Parenteral Packaging Sciences

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

Purpose:

We are seeking a highly skilled Scientist II to join our Global Material and Parenteral Packaging Science team, a core component of Product Development Science & Technology (PDS&T). The successful candidate will help drive the development of Container Closure Systems (CCS) for novel parenteral and biotechnological products (NBEs), supporting the advancement of some of AbbVie’s most strategic pipeline assets, including monoclonal antibodies, antibody-drug conjugates, and therapeutic toxins.

In this role, you will leverage your expertise in characterizing CCS—encompassing vials, prefilled syringes, and prefilled cartridges—with a strong focus on Container Closure Integrity (CCI). Your responsibilities will include conducting performance analyses using force analyzers, developing and validating analytical methods, providing technical support for CCS qualification in pharmaceutical manufacturing, and evaluating and implementing cutting-edge techniques.

Responsibilities:

• Planning, preparation, execution and evaluation of experiments for development of container closure systems of new parenteral drug products, namely liquid drug preparations of biotechnological drugs in vials, pre-filled syringes and cartridges as well as lyophilizates.
• Subject matter expert for the technical evaluation and implementation of CCI methods as well as continuous improvement based on a holistic CCI strategy and current regulatory requirements.
• Responsibility for development and validation of CCI methods according to GxP requirements.
• Responsibility for transferring ownership and maintaining lab equipment. Ensure required maintenance schedule, proper documentation, and training new users.