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Manufacturing Supervisor
Manufacturing SupervisorEli Lilly and Company • Indiana, PA, US
Manufacturing Supervisor

Manufacturing Supervisor

Eli Lilly and Company • Indiana, PA, US
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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're looking for people who are determined to make life better for people around the world.

Job Description Supervisor PFS11

The Filling Operations Teams are an essential part of Lilly's Kenosha County (LKC) Parenteral Manufacturing site. We manufacture and fill injectable parenteral products in state-of-the-art facilities to supply patients around the world. This position will work in a new facility with best in class, globally replicated production equipment.

Operations team members will work with the latest industry technologies, while learning from global teams, to manufacture key current parenteral products and preparing for upcoming products.

This role will be responsible for direct line supervision of operators, providing administrative leadership to filling operations team members, and developing technical expertise of employees. The leader will also assure quality behavior in the area and suggest technical improvements for delivery and operation of the areas.

This specific role will support PFS11, delivering new pre-filled syringe filling capacity to IPM.

Responsibilities :

  • Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
  • Ensure strict compliance with established policies / procedures (Safety, Production Procedures, Sanitization, Gowning, Etc.), ensure operators are trained appropriately.
  • Take ownership for implementation of countermeasures associated with audits, observations, inspection findings, and deviations.
  • Participate in planning of equipment prep, formulation and filling operations. Network with various areas to verify components and equipment are available for orders.
  • Identify / escalate issues to the Manager / Associate Director (if applicable).
  • Responsible for the coaching, development and performance evaluation of Operations personnel.
  • 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.
  • Responsible for shop floor execution as it relates to business plan, GMP conformance, and OSSCE.
  • Ensure adherence to use of proper technique in isolator and Grade C operational areas.

Basic Requirements :

  • High School Diploma / GED
  • Completion of Post Offer Exam, Completion of Work Simulation or Completion of Administrative Skills Testing if applicable.
  • 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.
  • Basic Preferences :

  • Ability to work cross-functionally with other areas of LKC Parenteral Manufacturing (Operations, Engineering, Maintenance, Quality, etc.)
  • Good interpersonal and communications skills to be able to work effectively in a team-based environment.
  • Previous parenteral manufacturing experience.
  • Strong understanding of quality systems in a manufacturing environment.
  • Flexible to work overtime, weekends, off-shifts.
  • Must be able to work a 3-2-2-3 shift schedule.
  • Additional Skills / Preferences :

  • Flexibility to support capital projects
  • Root Cause Analysis
  • Computer Proficiency
  • Leadership skills
  • Innovation and creativity
  • Teamwork / Interpersonal skills
  • Organizational skills
  • Attention to detail
  • Additional Information :

  • This role will be a 12-hour shift production schedule (3-2-2-3), 6am-6pm concurrent with scaleup and transition to production operations.
  • Project related travel may be required.
  • Applicant will work in various areas within LKC Parenteral where allergens may be present. Mobility requirements and exposure to allergens should be considered when applying for this 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 for further assistance.

    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.

    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).

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