Microbiologist - Technical Services/Manufacturing Sciences
The TS/MS microbiologist will ensure contamination control in the GMP production areas.
They will support the microbiological, viral and environmental monitoring programs at the Limerick manufacturing site.
The successful candidate will provide technical support for the facility startup and beyond in partnership with engineering, operations, quality control and quality assurance.
The role will provide support to up- and downstream processing areas for activities including EMPQ and preparation of strategy documentation including contamination FMEA, response plans, the product protection control strategy and investigations.
The successful applicant will have a deep technical expertise in microbiology and demonstrate strong data-driven decision-making and problem-solving capabilities.
They will also work to continuously improve process efficiency by implementing new technologies and process improvements.
They will maximize the benefits of a Digital Plant to gain in depth knowledge of the process through data analytics and Process Analytical Technology.
Key Responsibilities
Have an in-depth knowledge of the science of biotech manufacturing microbiological controls and associated analytical tests.
Understand molecule-specific control strategy and basis of specifications and critical quality attributes.
Work with the network and development organizations to ensure a well-understood, robust and fit-for-purpose microbial control strategy is developed and transferred.
Knowledge of virology controls required for mammalian cell culture, virus and mycoplasma analytical methodologies.
Support the EMPQ program, contamination FMEA and contamination response plan.
Creates, revises, or reviews documents such as SOPs, material specifications, protocols, and trend reports (water, environmental monitoring, etc) and performs investigations as needed.
Understand integration of process parameter requirements with MES/electronic batch records to ensure all regulatory, compliance and monitoring needs are captured in manufacturing electronic documentation.
Work as part of cross-functional teams, and establish partnerships with applicable functions, operations and TSMS Lab to understand interface between the science/engineering with the operations on the floor and bring deep technical expertise to the team.
Identify process improvements and participate in implementation of Lean manufacturing initiatives.
Understand and ensure compliance with safety, compliance, and regulatory expectations.
Contribute to the authorship and review of regulatory submissions and responses to regulatory agencies.
Basic Requirements
Degree or Masters based in microbiology or similar discipline.
Additional Requirements
Demonstrated technical capability with high productivity.
Proven track record of curiosity with learning agility.
Self-starter with high initiative and data-driven approach to problem-solving.
Demonstrated strong interpersonal skills.
Demonstrated strong verbal and written communication skills.
Demonstrated adaptability and flexibility to working in different environments, teams etc.
Demonstrated ability to participate in and facilitate decision-making.
Proficient in English.
Work Environment
These are 8-hour day roles.
As a manufacturing support function, the need for occasional evening or weekend support can arise.
Accommodation for Applicants with Disabilities
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions.
If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form at for further assistance.
Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
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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