QC Lab Technician (Lilly Contractor - Fixed Term)

Lilly del Caribe • Carolina, PR

7d • Onsite

About The Position

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Title: QC Lab Technician (Lilly Contractor - Fixed Term) Patients are at the center of everything we do at Lilly. We are currently hiring a QC Lab Technician This role supports critical work that helps bring medicines and solutions to patients responsibly and efficiently. #WeAreLilly

Requirements

• Associate degree (minimum) in science (preferably in Chemistry)
• 1 - 2 years of experience in GMP lab environment (preferably)
• Bilingual (Spanish/English)
• Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Responsibilities

• Responsible for receiving, analyzing, verifying and/or approving samples submitted to QCL following established procedures/methods.
• Responsible for preparing materials and conditioning equipment required for analyses, calculating results, and reporting them in the applicable systems.
• Participate in validation/transfer processes of analytical methods and instrument qualifications (including protocol preparation, execution, and final report).
• Ensure compliance with established analysis times and processes to deliver results on time.
• Support in investigative processes (e.g., generate investigative documents, participate in analytical investigations).
• Help implement and maintain quality controls in the laboratories.
• Comply on time with the training assigned to your position (cGMPs, EHS, DI).
• Participate in the process of training other resources, demonstrate team functioning, process and/or tasks in the area of responsibility.
• Participate in a team if required by supervision and/or voluntarily collaborate in teams of employees organized to achieve specific objectives.
• Assist in maintaining inventory of materials in the laboratory.
• Make appropriate use of materials and laboratory reagents.
• Keep the laboratory area clean, safe and organize.
• Report Environmental, Health and Safety (EHS) incidents to supervision as they occur.
• Use and care for personal protective equipment (PPE).

Benefits

• company bonus (depending, in part, on company and individual performance)
• company-sponsored 401(k)
• pension
• vacation benefits
• medical, dental, vision and prescription drug benefits
• flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• life insurance and death benefits
• certain time off and leave of absence benefits
• well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree