Lead Technician - Engineering - Day Shift

Initial Therapeutics, Inc.; Durham (NC); On-site; Full time

Job summary

An established industry player is seeking a dedicated Engineering Technician to support the launch of a cutting-edge Parenteral, Device, and Packaging Assembly Facility. This role involves providing technical expertise, ensuring equipment readiness, and collaborating with engineering and operations teams. You will play a crucial role in troubleshooting, process improvement, and maintaining safety standards in a dynamic environment. If you thrive in a fast-paced setting and are passionate about contributing to life-changing healthcare solutions, this opportunity is perfect for you.

Benefits

401(k) plan

Pension plan

Vacation benefits

Medical benefits

Dental benefits

Vision benefits

Prescription drug benefits

Flexible spending accounts

Life insurance

Employee assistance program

Qualifications

• Experience in a GMP manufacturing environment is essential.
• Solid experience in instrumentation, mechanical, and electrical disciplines required.

Responsibilities

• Support engineering initiatives and implement process improvement projects.
• Investigate and resolve issues with process equipment to minimize production delays.

Skills

GMP manufacturing experience

Instrumentation skills

Mechanical skills

Electrical skills

Troubleshooting skills

Microsoft Word proficiency

Microsoft Excel proficiency

Organizational skills

Interpersonal skills

Communication skills

Education

High School Diploma/GED

Tools

PLC programming

HMI programming

Computerized maintenance management systems

Studio 5000

FactoryTalk View SE

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.

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, transfer 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:

The Engineering Technician in Parenteral has the following objectives, but not limited to:

• Act as the first line of engineering support. Investigate and resolve issues with process equipment in 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.
• Coordination of 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.
• Implement tools for operations and engineering to learn and work more proficiently.
• Assist maintenance in:
  • Troubleshooting activities.
  • Job plans reviews.
  • Participating in periodic reviews of equipment state.
• 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 a pharmaceutical manufacturing.
• Solid experience in a GMP manufacturing environment.
• Solid experience in instrumentation, mechanical, and electrical disciplines.

Additional Preferences:

• Demonstrated ability to work safely in a participative environment.
• Knowledge of Inspection and Robotics 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.
• Experience in PLC and/or HMI programming.
• Studio 5000 and FactoryTalk View SE programming experience.

Other Information:

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

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.lilly.com/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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

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

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for 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; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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