Operations Supervisor - Formulation (Night Shift)

Eli Lilly and Company; Durham (NC); On-site; USD 60,000 - 95,000; Full time

Job summary

Join a forward-thinking global healthcare leader as an Operations Supervisor for Parenteral Formulation. This exciting role involves managing multiple shifts in a dynamic manufacturing environment, ensuring adherence to safety and quality standards while leading a diverse team. You'll be instrumental in supporting start-up activities and operational excellence, making a significant impact on the production of life-changing medicines. If you're passionate about improving lives and thrive in a fast-paced setting, this is the perfect opportunity for you to grow and lead in a meaningful way.

Qualifications

• High School Diploma required; Bachelor's in science or engineering preferred.
• Experience in operations supporting pharmaceutical manufacturing is a must.

Responsibilities

• Manage two shifts on a rotating 12-hour schedule for formulation activities.
• Ensure a safe work environment and maintain quality processes.

Skills

Leadership

Communication Skills

Technical Aptitude

Lean Manufacturing Principles

Root Cause Analysis

Manufacturing Execution Systems

Organizational Skills

Interpersonal Skills

Education

High School Diploma

Bachelor’s Degree in Science or Engineering

Tools

Manufacturing Execution Systems

Desktop Software

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.

Operations Supervisor – Parenteral Formulation (Night Shift) will support start-up activities for multiple suites at the RTP manufacturing site. The position will be responsible for managing two shifts on a rotating 12-hour schedule. The teams will be primarily supporting dispensing and formulation activities with supplemental support tasks for parenteral material preparation.

Key Objectives:

1. Support Site Leadership to build a diverse, inclusive, and capable site organization by delivering area operational procedures, quality processes and controls for Parenteral areas.
2. Responsible for hiring/managing 12+ direct reports (3 per shift and suite) working across 2 formulation suites.
3. Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE goals.
4. Ensures adequate qualified/trained staffing for operators working on the manufacturing lines.
5. Communicate with the area Manager on quality, equipment, and operational issues and areas for improvement.
6. Responsible for the coaching, personal development, and performance evaluation of operators/technicians.
7. Originate/Investigate deviations or operational quality issues.
8. Collaborate with support functions to achieve a consensus for unexpected events during manufacturing.
9. Collaborate with support functions to Standard Operating Procedures.
10. Act as both administrator and technical leader for operations, setting a good example through demonstrated knowledge of procedures, compliance with quality systems and use of proper technique.
11. Responsible for shop floor execution as it relates to business plan, current Good Manufacturing Practice (CGMP) conformance and Operational Standards for Supply Chain Excellence (OSSCE).

Basic Requirements:

• High School Diploma or equivalent
• Previous experience in operations or directly supporting a pharmaceutical manufacturing operation.

Additional Skills/Preferences:

• Bachelor’s Degree in science, engineering, or technical field
• Previous experience in facility/area start-up environments
• Previous experience with Manufacturing Execution Systems and electronic batch release.
• Experience with root cause analysis, technical writing / authoring investigations
• Knowledge of lean manufacturing principles
• Demonstrated leadership experience
• Skills in providing/receiving feedback and creating employee development plans
• Basic computer skills (desktop software) are required.
• Solid understanding of FDA guidelines and CGMP requirements.
• Excellent interpersonal, written and oral communication skills
• Strong organizational skills and ability to handle and prioritize multiple requests.
• Strong technical aptitude and ability to train and mentor others.
• Ability to adjust their schedules to meet milestones and to support both teams.
• Ability to work in a controlled environment (classified and non-classified) which requires specific company provided gowning.
• Ability to wear safety equipment (safety glasses, safety shoes, protective gloves etc.)

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.

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.

Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly