At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

BASIC REQUIREMENTS:

• Hons BSc in Analytical Sciences (Chemistry, Biochemistry, Microbiology) with a minimum of 3 years pharmaceutical experience.
• Comprehensive knowledge of quality control operations with an emphasis on techniques such as immunoassays, quantitative PCR, chromatography, capillary electrophoresis and spectroscopy.
• Proficiency in the use of multiple instrument platforms (e.g. Agilent, Beckman Coulter, Sciex, Molecular Devices, Applied Bioscience, etc.) and associated software applications (e.g. SoftMax Pro, Empower, Accuseq LIMS / LES systems)

ADDITIONAL SKILLS/PREFERENCES:

• Excellent attention to detail in all aspects of the work.
• Demonstrated understanding of Data Integrity and its application in a Digital Laboratory.
• Highly competent with computer systems.
• Experience working in cross functional teams and proven ability in decision making.
• Demonstrated ability in critical thinking, data analysis, problem solving and experience in root cause analysis.
• Strong organizational skills, including ability to follow assignments through to completion.
• Self-motivated, positive and ability to work under pressure.
• Demonstrates flexibility and adaptability to meet business needs.
• Excellent interpersonal and communication skills (written and oral).
• Demonstrates a continuous improvement mind-set.
• Demonstrated initiative – able to work proactively without direct supervision.
• Demonstrated ability to implement changes in technology and business systems / processes.

• Executing analytical procedures in accordance with current corporate specifications and cGMP’s and for maintaining the relevant SOP’s.
• Building / Maintaining QCL digital systems in collaboration with site and external Digital teams.
• Reporting results into a computer storage system (LIMS), as well as performing testing using automated systems.
• Involved in the qualification of analytical instruments and in their routine maintenance.
• Development, validation and verification of new methodologies, as part of new product introductions or process improvement activities.
• Recognizing atypical assay behavior and normally encountered equipment failure.
• Involved in deviation investigations and will record any errors encountered, as per procedures and training.
• Following all relevant Environmental, Health and Safety procedures and involved in incident investigations as required.
• Responsible for the maintenance of an inventory of chemicals and supplies used to perform analytical testing.
• Assisting in the training of other personnel and as their level of skill develops, may be responsible for the full training of other Laboratory personnel.
• Responsible for adhering to, and improving, where appropriate, safety procedures to protect their other personnel and company property.
• Displaying a high level of integrity in the performance of their work.
• Relating well to other people with whom they come in contact, both within and outside of the laboratory area.
• Knowledgeable of general scientific methods and capable of learning and executing new techniques and instrumentation after appropriate training.
• May also be requested to partake in or lead area or cross-functional continuous improvement projects e.g. Six Sigma or other appropriate methodology