Lilly
healthcare
SeniorLaboratoryAnalyst(Sr.Specialist-Analytical)
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“Senior Laboratory Analyst (Sr. Specialist - Analytical) at Lilly. Skills: Analytical Sciences, quality control operations, analytical instruments, methodologies development, validation, verification. 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”
What You'll Achieve.
safety and quality improvements; increased productivity; variability reduction
Industry & Context.
Recognizing atypical assay behavior and normally encountered equipment failure; deviation investigations; critical thinking; data analysis; problem solving; root cause analysis
Candidates must be able to travel for familiarization and training as required, May be required to work on a shift basis depending on production support needs
What They're Looking For.
Must Have
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)
Nice to Have
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, 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
What You'll Do.
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
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
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
How You'll Work.
Team & Collaboration
Building / Maintaining QCL digital systems in collaboration with site and external Digital teams; Experience working in cross functional teams; Relating well to other people with whom they come in contact, both within and outside of the laboratory area
Communication Scope
Excellent interpersonal and communication skills (written and oral)
Process & Methodology
partake in or lead area or cross-functional continuous improvement projects
Full Job Description
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. **Organization Overview:** Lilly is designing and building a Next Generation Biotech Drug Substance Manufacturing Facility in Limerick, Ireland. This is an exciting opportunity to help build and operate a state-of-the-art manufacturing site from the ground up. Our new Limerick facility will be one of Lilly’s most technically advanced manufacturing sites and will include next-gen manufacturing technologies, and advanced data collection and analysis platforms that will result in safety and quality improvements, increased productivity, and variability reduction. **Responsibilities:** The **Senior Laboratory Analyst (Sr. Specialist - Analytical)** key responsibilities shall include but shall not be limited to: * 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 encoun
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