Sr. Scientist I, Combination Products

Sr. Scientist I, Combination Products Full-time Company Description 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 . Job Description Conceive and implement novel experimental approaches to answer scientific questions. Investigate, identify, develop, and optimize new methods and techniques. Contribute to project science in area of expertise. Develop productive collaborations and communications with other groups across science disciplines. Responsibilities Technical support of produce development and leadership at lab study scale up for commercial manufacturing of medical devices, drug device delivery systems, and combination products. Cross-function engagement and team matrix working experiences in portfolios of drug delivery system product development projects. Advances in scientific and engineering of medical device related experimental DOE design of experimental activities for the engagements with internal teams and external partners. Supports the experimental lab execution, data generation and collection, results summary and slide deck preparation and presentation at weekly meeting. Interface engagement of the project cross-function team and governance process and forward-looking evaluation of potential risk with timely problem solving. Supports in tech transfer, process development, optimization, and scale-up activities. Work closely with contract manufacturing organizations (CMOs) to ensure technical and operational alignment with company standards. Plans, designs, executes, documents, and analyzes a regimen of tests to evaluate, verify and/or validate a system. Provide knowledge in pharmaceutical manufacturing processes, particularly small molecules and biological drug related device delivery systems and combination products Interface with project and laboratory teams to develop DOE and functional tests, experimental protocols, and new target evaluations. Assesses risks and creates test plans around risk priorities; analyzes results, states conclusions, and assesses residual risks after tests are complete; in addition, assesses adequacy of support for conclusions by test results. Understands regulations, apply guidance and standards on design verification and design validation to test activities and work products; prepares documentation for compliance with standard operating procedures. Develop and review technical documentation, including standard operating procedures (SOPs), batch records, and validation protocols. Troubleshoot manufacturing challenges and support investigations into deviations or process failures. Collaborate cross-functionally with marketing, quality, regulatory, and supply chain teams to ensure seamless operations. Stay up to date with industry trends and best practices in pharmaceutical product development and lab, pilot and scale up manufacturing and commercial production. Qualifications Preferred Ph.D. degree with 3-5 years of industry working experience in device-drug delivery system and combination product is preferred; post-doctor experience and high quality of Ph.D. candidates, and/or MS with 5-10 years of working experience in the field of biomedical, mechanical, chemical, materials science and engineering, biotechnology, and pharmaceutical and other related engineering fields. Experience in developing medical devices, device-drug delivery systems, and/or combination products. Broad experience in product and process design, development, design verification and design validation and patient usability applications. Prior