Process Technician - Formulation

Organization Overview:

We serve an extraordinary purpose. For more than 140 years, we have worked to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world’s greatest health challenges. We explore how next generation therapeutics, new technologies, and data analytics can improve patient health and the healthcare system. Our team shares a real passion for challenging conventional wisdom and creating an environment that embraces creative, break-through concepts.

One of the most recent actions Lilly has taken is designing and building a new, modern, and groundbreaking facility in Raleigh-Durham North Carolina! This is an exciting opportunity to help build a facility which will manufacture, assemble, and package parental drug products.

Quick Benefits 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.

Responsibilities:

• Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision.
• Attain and maintain qualification for the operation of assigned process equipment and duties in the area.
• During the project phase, the Operator/Technician will support commissioning/qualification activities required to bring formulation suites into service as well as supporting site operational readiness activities. This position may require domestic travel with the potential of international travel based on program need.
• Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleanings, etc.).
• Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.
• Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
• Must be willing to work 12-hour shifts (2-2-3 schedule)
• Identify opportunities for operational improvements.
• Currently in the startup phase of operations. Candidate must be flexible and be willing to perform non-routine work with Safety & Integrity in mind at all times
• Support Site Leadership to build a diverse and capable site organization by delivering area operational procedures, quality processes and controls for the Parenteral Formulation area.
• Adhere to RTP Plant safety policies and procedures, contribute to a safe work environment.
• Assists in checking execution documentation (PMX, SAP, Cleaning Logs, etc.)
• Provide commissioning, qualification, and operational readiness support during project phase.
• Drives key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
• After project phase completion, this role will be responsible for execution of daily operations tasks defined by the shift lead/supervisor.

Basic Requirements:

• Must pass a “fitness for duty” physical exam.
• High School Diploma or equivalent.

Additional Preferences:

• Basic digital literacy (desktop software) is required.
• Ability to effectively communicate (written and verbal).
• Flexibility and problem-solving skills.

• 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.
• Project phase will require a baseline 5-day work week with flexibility to adjust hours to support specific project tasks.
• Ability to work 12-hour shifts on days (2-2-3 schedule) with additional overtime as the need arises.
• Ability to wear safety equipment required (safety glasses, safety shoes, protective gloves etc.).
• Ability to gown and work in controlled classified areas (grade c and grade d).
• The position is for the Lilly Research Triangle Park site and during the project phase will allow for a flexible working environment which includes working remotely in a limited capacity with manager approval.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( [email protected] ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.