Lilly

healthcare

SeniorLaboratoryAnalyst(Sr.Specialist-Analytical)

Limerick, Ireland FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“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.

healthcare
Problems you'll solve

Recognizing atypical assay behavior and normally encountered equipment failure; deviation investigations; critical thinking; data analysis; problem solving; root cause analysis

Eligibility Requirements

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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