Process Technician - Quality Assurance Floor Support (Day Shift)

Eli Lilly and Company; Durham (NC); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player seeks dedicated individuals to ensure quality and safety in operations. This role involves mentoring teams, ensuring compliance with good documentation practices, and actively participating in quality checks and inspections. The company offers a supportive environment where employees can thrive and contribute to life-changing medicines. With a focus on collaboration and quality culture, this position is ideal for those looking to make a significant impact in healthcare. Enjoy benefits starting from day one, including medical, dental, and a generous sign-on bonus. Join a team committed to making life better for people worldwide.

Benefits

Medical Benefits

Dental Benefits

Vision Benefits

Prescription Benefits

Paid Vacation

Sign-On Bonus

Qualifications

• High School Diploma required; Bachelor's preferred in relevant fields.
• Strong decision-making and problem-solving skills are essential.

Responsibilities

• Ensure compliance with safety and quality standards in operations.
• Lead and mentor teams on quality matters and GMP programs.

Skills

Decision Making

Problem-Solving

Attention to Detail

Communication Skills

Teamwork

Education

High School Diploma

Bachelor’s Degree in Science or Engineering

Tools

SAP

Darwin

Inventory Management Systems

Job 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.

Key Objectives/Deliverables:

• Responsible for adhering to safety rules and maintaining a safe work environment for both you and others by supporting HSE corporate and site goals.
• Responsible for ensuring training is completed and remains in compliance. Communicates with Quality Specialist Lead and QA Floor Support Supervisor on quality and operational issues.
• Ensures adherence and understanding of good documentation practices and compliance with applicable procedures for both Operations and Support personnel.
• Lead, mentor, and coach Operations, and support personnel on quality matters, while driving the site Quality culture.
• Ensures regular presence in device assembly and packaging areas to monitor GMP programs and quality systems.
• Reviews and approves GMP documentation in support of daily operations such as: Electronic Logs, and Other documents as required.
• Performs daily Quality Checks.
• Troubleshoot and provide QA systems support to reconcile issues in multiple systems (i.e., SAP, EWM, Darwin and other systems as required).
• Participate in self-led inspections and provide support during internal / external regulatory inspections.
• Perform collection, visual inspection and delivery of samples both in person and Electronically (Darwin).
• Ability to work cross functionally and work collaboratively with all levels of the organization.

Basic Requirements:

• High School Diploma or equivalent.
• Must pass a vision exam and be free of color blindness.
• Must be equivalent to 20/20 correctable close vision acuity.
• Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.

Additional Preferences:

• Bachelor’s degree in a science, engineering, computer, or pharmaceutical related field of study, preferred.
• Completion of Post Offer Exam or Completion of Work Simulation if applicable.
• Demonstrated decision making and problem-solving skills.
• Strong attention to detail.
• Proven ability to work independently or as part of a team to resolve issues.
• Ability to work overtime, as requested.
• Demonstrated strong oral and written communication and interpersonal skills.
• Demonstrated knowledge and understanding of manufacturing process and Quality Systems.
• Proficiency with inventory management systems and deviations systems, (i.e. SAP, Darwin, etc.).
• Previous work with combination products or devices with experience with US/EU regulations and notified bodies.
• Previous experience in GMP production environments.
• Previous facility or area start up experience.
• Knowledge of Validation / Qualification activities.

Additional Information:

• May be required to respond to operational issues outside of core business hours / days.
• Applicant may work in various areas within the DAP and Warehouse buildings. Mobility requirements should be considered when applying for this position.

Quick Benefit Overview:

• Medical, Dental, Vision, Prescription benefits are effective on your first day of employment.
• Paid vacation- starting annually at 120 hours (prorated based on start date).
• $3,000+ sign-on bonus.