Associate, Scientist II Analyst Chemist

Company Description

About Abb Vie

Abb Vie'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 Abb Vie, please visit us at  Follow @abbvie onLinked

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Abb Vie Analytical Research & Development (Analytical R&D) is a global analytical scientific organization responsible for all CMC analytical activities related to the development of Abb Vie's pharmaceutical products.

Our scope includes Abb Vie's diverse pipeline of innovative small molecule medicines and spans from the selection of Discovery candidate molecules to Late Stage Clinical.

We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance Abb Vie's pipeline of innovative medicines.

Careers in Abb Vie Analytical R&D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies.

We are looking for diverse candidates with strong scientific experience to join the Abb Vie Analytical R&D team and can offer exciting and rewarding career opportunities for these candidates.

For the Associate Scientist II position, we are seeking a highly motivated candidate who can independently generate precise, reliable and reproducible data in a timely manner. Can demonstrate experimental precision and strong data interpretation skills. They should possess understanding of core discipline and support early phase development of New Chemical Entities (NCEs) drug substance and drug product in both preclinical and clinical programs.

Collaborate within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), and Quality Assurance (QA) and CMC-Regulatory.

Responsibilities:

• Independently plan and perform routine tasks competently within a timely fashion and generate precise, reliable and consistent results.
• Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.
• Documentation of experimental activities and results in a GMP compliant fashion using an electronic data acquisition and management systems.
• Analyze and critique results, noting significant deviations from the expected results.
• Troubleshoot experiments and instrumentation.
• Learn and understand new experimental techniques with a curiosity to apply them for unique project / assignment requirements.
• Demonstrate