Associate - QC Laboratory Support
at Lilly
5SF, Toscana, Italy -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Nov, 2024 | Not Specified | 03 Sep, 2024 | N/A | Manufacturing Processes,Salary Review,Analytical Skills,Management Skills,English | No | No |
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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.
Eli Lilly Italia is seeking a QC Laboratory Support Associate to lead cross-functional projects in the Tech Agenda, focusing on laboratory instrumentation and systems.
As the Laboratory Secondary Loop Coordinator, you’ll be the go-to expert for all things related to lab instrumentation and systems. You’ll ensure that the introduction, qualification, and updates of lab equipment and systems comply with company procedures, pharmacopeias, GMP standards, and applicable GQS/LQS. Your role is crucial in maintaining GMP and corporate standards within your assigned area.
REQUIREMENTS:
- Master’s degree in Engineering or Technical/Scientific disciplines (e.g., Chemistry and Pharmaceutical Technologies)
- Understanding of manufacturing processes, GMP regulations, and international pharmaceutical standards.
- Strong analytical skills for data/results analysis
- Fluent in English
- Problem-solving and decision-making skills
- Proactivity and autonomy
- Planning, prioritization, and unexpected event management skills
- Continuous Improvement mindset
Responsibilities:
KEY RESPONSIBILITIES:
- Lead and coordinate lab instrumentation and systems projects, ensuring timely implementation.
- Assist laboratory Process Teams with the introduction of new lab instruments and system upgrades.
- Ensure GMP, GQS/CQP, and pharmacopeia standards are applied within your area of expertise.
- Maintain an appropriate escalation process.
- Handle investigations related to deviations in your area.
- Approve procedures within your scope.
- Approve qualification and requalification documentation for lab instruments (IOQ, PQ, QP, etc.).
- Independently manage complex instrumentation/equipment projects.
- Propose and oversee changes in your sector.
- Potentially act as System Owner for computerized systems.
- Assist in managing budget expenses and capital expenditures.
- Ensure continuous improvement in your area of expertise.
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.
- Annual Salary Review: We recognize and reward your continued effort with an annual salary review, providing opportunities for advancement based on your performance. As part of our commitment to your future, you may also be eligible to receive a stock option package, aligning your success with the company’s growth
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Chemistry, Engineering
Proficient
1
50019 Sesto Fiorentino, Italy