AbbVie · Sydney
Manufacturing & OperationsFull-timeposted 7d ago
About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
The job that makes possibilities real in patients' lives. And yours.
The job that helps you get ahead in life. Moving mountains together.
Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrow’s unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities for developing and increasing your own skills? You’ve come to the right place!
Moving mountains together – as Post-Doc – Innovative manufacturing concepts on Biologics (all genders)
Early Manufacturing Process Development (EMPD) within Biologics Drug Product Development is responsible for developing robust manufacturing processes for AbbVie's parenteral pipeline projects, supporting the advancement of biologics through early clinical stages. Biologics are often co-administered with other biologics to boost their clinical efficacy and the overall patient experience, while requiring multiple injections. Formulating both active ingredients into a single drug product significantly strengthens patient compliance and dose accuracy. This goes along with additional technical challenges for drug development and manufacturing, which will become your primary topics of interest through the upcoming 24 months. You will design, execute and assess studies to identify key risks and their mechanisms for co-formulating biologics during drug product development and manufacturing, comprising identified unit operations as well as in-process controls to enable a state-of-the-art, compliant and robust control strategy while maintaining maximum dose-range flexibility.
Responsibilities
Here's how we can move mountains together
At multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.
At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.
Any questions? Feel free to email TalentAcquisition.de@abbvie.com – We look forward to hearing from you!
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.html