ASSOCIATE – QC BIOLOGICAL LAB

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.
We are currently seeking a QC Biological Lab Associate to join our Quality Control team at the Sesto Fiorentino manufacturing site.
This role is responsible for the analytical release of products within the assigned area of expertise and for providing high-level technical support in the execution of daily laboratory activities.
The successful candidate will also play a key role in identifying and implementing continuous improvement initiatives within the lab environment.
Key Responsibilities.
Ensure the application and compliance with GMP regulations within the laboratory, specifically in areas of assigned responsibility.
Provide expert-level analytical and technical support to daily QC operations.
Monitor and ensure that analytical methods are in compliance with validation data, regulatory dossiers, pharmacopoeias, and GMP standards.
Act as primary point of contact for analytical method qualification processes.
Coordinate laboratory projects and changes under assigned responsibility.
Conduct and review laboratory deviation investigations, ensuring robust and technically sound justifications.
Referente principale per la stesura della reportistica periodica relativa alle attività del laboratorio biologico Primary contact for drafting periodic reports on biological lab activities.
Authorized to release analytical results within assigned scope.
Author and review SOPs and analytical methods for relevant areas of responsibility.
Support and engage in international initiatives related to the assigned quality control area.
Key Competencies Master’s degree in a scientific discipline (e.
., Biological Sciences, Biotechnology, or related fields).
A completed PhD will be considered a strong plus.
Proficient in English (minimum level.
B2).
Solid knowledge of microbiology and analytical testing techniques.
Previous laboratory experience in pharmaceutical or biotechnology environments.
Familiarity with GMP and GLP regulations.
Strong team-oriented mindset with good interpersonal and communication skills.
Proactive and autonomous with the ability to manage priorities Continuous improvement mindset and ability to propose innovative solutions What we offer.
Step into a role where your expertise is recognized, appreciated, and rewarded.
As a member of our team, you can expect.
Competitive Salary.
We offer a competitive base salary supplemented by an annual variable component based on achieving objectives.
Relocation Package.
You will be eligible for a relocation package based on your location.
Comprehensive Benefits.
Enjoy a well-rounded welfare package, including an extensive insurance plan.
This position requires working on-site, and includes 4 days of remote work per month.
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 (https://careers.
illy.
om/us/en/workplace-accommodation) 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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