Senior Scientist I, The Parenteral And Eyecare Product Development S&T

Job Description
The PDS&
T Parenterals/Eye Care group is seeking a motivated Senior Scientist as a CMC drug product project lead, specifically for parenteral drug product process development and commercial site scale up and tech transfer. The candidate will independently design and execute lab studies to develop robust manufacturing processes for clinical phase and commercial products. This person will generate and analyze precise, reliable, and reproducible data in a timely manner, independently or under the direction of a more senior scientific leader. This position will be an integral part of the product development and CMC teams and is highly collaborative across functions such as analytical, process engineering, internal and external manufacturing, quality assurance, supply chain and Operations Manufacturing Sites.
Independently design and conduct critical experiments that further project goals. Implement and may innovate new experimental protocols/techniques.
Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.
Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.
Authoring of comprehensive, scientifically sound reports, e.G. development reports or risk assessments that serve as source documents for regulatory submissions. Author portions of regulatory submissions to designated health authorities related to these reports.
Develop and maintain comprehensive project plans, timelines and development and/or scale up tech transfer strategy;
technical projects at all stages of development are included, from phase II clinical through commercial.
Lead cross-functional PDS&
T product teams and represent the CMC team and/or PDS&
T in interface with PDS&
T leadership, other Operations functions, other AbbVie functions and external partners. Participate in or coordinate Governance efforts such as Product Performance Teams or gate reviews.
Prepare and review submissions through registration of the product as well as post-approval life-cycle management. Serve as a peer reviewer for submissions and under stand how regulatory submissions limit operational changes.
Establish and foster partnerships with key customers and counterpart functions to facilitate effective collaboration. Identify and promote best practices among PDS&
T CMC leads.
Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.