Lead Technician - Engineering - Night Shift

Eli Lilly and Company; Durham (NC); On-site; Full time

Job summary

Join a forward-thinking company dedicated to improving lives through innovative healthcare solutions. As an Engineering Technician, you will play a pivotal role in establishing a state-of-the-art Parenteral, Device, and Packaging Assembly Facility in Raleigh-Durham, North Carolina. This position offers an exciting opportunity to contribute to the development of cutting-edge manufacturing processes and ensure equipment reliability. You will collaborate with a talented team, applying your technical expertise to enhance production efficiency and safety. If you are passionate about making a difference in the pharmaceutical industry, this role is perfect for you.

Qualifications

• Experience in GMP manufacturing and supporting pharmaceutical production.
• Knowledge of instrumentation, PLC, and HMI programming.

Responsibilities

• Provide engineering support to production processes and resolve equipment issues.
• Implement process improvement projects and maintain equipment readiness.

Skills

GMP manufacturing experience

Instrumentation knowledge

Mechanical skills

Electrical skills

PLC and HMI programming

Process troubleshooting

Interpersonal skills

Organizational skills

Education

High School Diploma/GED

Tools

Studio 5000

FactoryTalk View SE

Computerized maintenance management systems

Microsoft Word

Microsoft Excel

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.

Compensation:

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $31.37 - $52.28.

Lilly is designing and building a new state-of-the-art Parenteral, Device, and Packaging Assembly Facility in Raleigh-Durham, North Carolina. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up.

Responsibilities:

The Engineering Technician in Parenteral delivers solid technical expertise as the first line of engineering support to production processes, transfers knowledge of equipment capabilities, and works in conjunction with other engineering team members, as well as operations and maintenance departments to ensure process equipment readiness and reliability. The Engineering Technician is responsible for equipment performance by supporting engineering initiatives and implementing process improvement projects. This position requires expertise in production processes, commissioning, qualification, and validation of assets. This position will help ensure that equipment is maintained in a qualified state, can be operated safely, and maintenance is properly performed on the systems.

Key Objectives/Deliverables:

• Act as the first line of engineering support. Investigate and resolve issues with process equipment in Filling, Formulation, Equipment preparation, Inspection, and Robotics that create production delays.
• Transfer knowledge of equipment capabilities and operational techniques to operators and maintenance.
• Implement tools for operations and engineering to learn and work more proficiently.
• Coordinate engineering contractors and vendors.
• Work closely with process and automation engineers to assist during qualification, engineering studies, cycle development, investigations, and process changes, providing technical reports, redlining drawings & specifications.
• Work closely with other technicians to identify and troubleshoot mechanical, electrical, automation, and instrumentation issues.
• Identify opportunities for process improvements using equipment performance data and communicate to process and/or automation engineers.
• Plan and execute small projects for process and automation equipment improvements.
• Work with the process area owners and operations personnel in development of equipment design, procedures, engineering studies, and maintenance practices that will enable the process to operate as required.
• Find and eliminate safety issues with the equipment and processes.
• Execution of Pre-Start Up Safety (PSSR) reviews.
• Participate in safety reviews and audits, as required.
• Perform activities in accordance with GMPs and applicable procedures.
• Understand the production process and critical process parameters.
• Assure that operational and maintenance procedures and practices reflect safety concerns.

Minimum Requirements:

• High School Diploma/GED
• Previous experience directly supporting pharmaceutical manufacturing.
• Solid experience in a GMP manufacturing environment.
• Solid experience in instrumentation, mechanical, and electrical disciplines.
• Experience in instrumentation, PLC and/or HMI programming.
• Studio 5000 and FactoryTalk View SE programming experience.

Additional Preferences:

• Demonstrated ability to work safely in a participative environment.
• Knowledge of Filling, Isolator, Autoclaves, Parts Washers, Inspection equipment and other Parenteral manufacturing operations.
• Strong equipment/process troubleshooting skills.
• Demonstrated proficiency with Microsoft Word and Excel; proficient at typing and writing technical documents.
• Demonstrated ability to work independently with strong organizational skills and attention to detail and ability to adapt to rapidly changing priorities.
• Demonstrated strong interpersonal skills and communications skills with a service attitude.
• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
• Previous experience with highly automated equipment.
• Knowledge of Parenteral equipment and manufacturing operations.
• Experience with computerized maintenance management systems.

Other Information:

• Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, etc.).
• Role will be responsible to work 12-hour shifts on nights (2-2-3 schedule).