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 (https://www.tiktok.com/@abbvie) . Job Description + Provides support in manufacturing activities during the technology transfer, qualification and validation batches associated with new product introductions to the site. + Provides technical expertise related to manufacturing process and equipment in response to deviations and design of experiment to understand and eliminate the root cause(s). + Support investigations from chemistry/process perspective for product complaints and deviations. + Identify and develop necessary laboratory experiment for continuous improvement projects. Work closely with process engineers and other departments to deliver these continuous improvement projects including change control management. + Participate in PHA and quality risk assessment activities providing relevant technical knowledge related to process chemistry and safety. + Actively participate to collaboration and learning of best practices with external subject matter experts (SMEs) including GPRD, MS&T on process development for suitable future product introduction. + Provides support to regulatory filings and cGMP audit activities. + Authors technical reports, batch records, SOP’s, investigations, protocols as required and ensures consistency and quality of the group’s documentation in compliance with company guidelines. + Any other duties as assigned by supervisor. Qualifications + Bachelors/Masters/PhDs degree In a technical/science field, including Chemistry, Biochemistry or Pharmaceutical Sciences. + 0-6+ years (bachelor)/0-4+years (Master)/0-2+ year (PhD) technical experience in process chemistry, pharmaceutical manufacturing process, tech transfer, commissioning and validation in pharmaceutical industry. + Knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is preferred. + Demonstrated process development skills, including the ability to deliver innovative process chemistry at scale. + Proven records in facilitating the successful transition from laboratory to full scale production. + Experience of start-ups and new product introduction to commercial facilities is preferred. + Good problem solving skills, embrace problem solving tools like FMEA, 5 Why, able to work under pressure and tight timeline. + Team player, highly self-motivated and able to work under minimum supervision. 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