Qcl Shift Analyst

Overview
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.
Position
Position Title:
QCL Shift Analyst (Full Rotation), IE2b (peptide manufacturing facility).
Reporting to:
Supervisor - Analytical.
Contract:
24 month fixed term contract
Overview
We currently have an opening within the QCL Peptides team for a Full Rotation QCL Shift Analyst supporting IE2b, the peptide manufacturing facility.
Main purpose/objective
To support IE2b (peptide manufacturing facility) QCL Operations.
The IE2b QCL Shift Analyst will operate on a 24/7 basis to support peptide manufacturing operations.
Qualifications
Educational Requirements:
B.Sc.
in Analytical Chemistry or other related discipline.
Responsibilities
Support all aspects of IE2b operations: processing, cleaning, Process Analytical Technology (PAT) and data review.
Execute online, at-line and offline analytical testing, to support manufacturing.
Perform analytical techniques in chromatography, including HPLC, Agilent UPLC, Waters PATrol UPLC and GC, spectroscopic methods, and wet chemistry techniques, etc.
Function as technical resource (Subject Matter Expert) for analytical technologies related to the peptide manufacturing process and train other analysts in this area of expertise as required.
Respond appropriately to equipment failures (including laboratory and on the floor instrumentation) to minimize process down time, including enacting business continuity procedures.
Perform primary review and second person verification of process data and results and trend analysis, including process monitoring (PAT review) and fast processing of data.
Conduct and document laboratory investigations to completion.
Maintain the laboratory facility, equipment and on the floor process analytical equipment in an inspection-ready state.
Liaise with other functions (Quality Control, Quality Assurance, Operations, Automation, Technical Services and Facilities, etc.) and contractors, as necessary.
Communication during handover to other shifts, as to the testing/equipment status and details of any issues/problems that have occurred.
Actively participate in assigned laboratory and building processes such as, safety audits, procedure revision, housekeeping, and improvement projects.
Key Attributes
Strong understanding of safety hazards, basis of safety and risk assessment and an ability to react appropriately.
Strong technical aptitude and have a willingness to learn new tasks/technology.
E-Systems competency and knowledge of Empower.
Experience with process analytical technologies, HPLC/UPLC and GC an advantage.
Proven ability to work independently in a fast-paced environment, own tasks and training, problem solve/troubleshoot and adapt to changing priorities.
Strong collaborative skills with an ability to work effectively in a team environment.
Excellent communication (written, oral, listening) skills.
Excellent attention to detail and accuracy in execution.
Customer focus; takes personal responsibility for speed; quality and accuracy of delivery.
Self-motivated, positive and ability to work under pressure.
Note
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability, or any other legally protected status.
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