Production Specialist

1 month ago


Pleasant Prairie, Wisconsin, United States Lilly Full time

At Lilly, we are dedicated to making life better for people worldwide. Our company is a global healthcare leader with headquarters in Indianapolis, Indiana. As part of our team, you will be working towards discovering and delivering life-changing medicines to those who need them. We prioritize the understanding and management of diseases, giving back to our communities through philanthropy and volunteerism.

We seek individuals who are determined to make a positive impact on people's lives.

About the Role:

The Production Specialist will be based in the Kenosha County (Pleasant Prairie) Parenteral Manufacturing site. The primary goal of this position is to ensure the safe inspection of high-quality pharmaceutical products by following good manufacturing practices in controlled facilities. You will operate various automated and semi-automated equipment in manufacturing areas, performing manual inspections while adhering to Lilly's culture of integrity, excellence, and respect for people.

This role requires occasional travel to collaborate, train with, and learn from sites that produce our medicines.

Key Responsibilities:

  • Maintain a safe work environment by adhering to Parenteral Plant safety policies and procedures.
  • Set up and operate non-aseptic manufacturing processes, including the use and operation of automated and semi-automated inspection machines in controlled facilities.
  • Follow standard operating procedures, current Good Manufacturing Practices, and safety policies/procedures.
  • Document process steps on appropriate batch documentation.
  • Participate in department meetings, team building, and training activities.
  • Contribute to the development of department SOPs and training.

Requirements:

  • Prior experience working in a manufacturing environment.
  • Pass a post-offer physical exam.
  • Pass an eye exam and not be color blind.
  • Authorization to work in the United States without employment visa sponsorship.

Preferred Qualifications:

  • Experience with GMPs.
  • Ability to work through production issues, including basic troubleshooting skills and tool usage.
  • Familiarity with PMX, Flow-stream, or other electronic batch documentation systems.
  • Previous pharmaceutical manufacturing experience.
  • Manual, automated, and semi-automated inspection experience.
  • Strong attention to detail in carrying out manufacturing conduct and technique.
  • Basic math skills, including data evaluation.
  • Basic computer skills, including HMIs and other computer terminals used to monitor equipment status and document production activities.
  • Excellent documentation skills.
  • Proven teamwork skills in setting up, running, and changing over manufacturing lines.
  • Responsibility for maintaining a safe work environment, working safely, and supporting Health and Safety Corporate and site goals.

Education Requirements:

  • High school diploma or equivalent.

Compensation:

The estimated annual salary for this position is $65,000 - $85,000, depending on qualifications and location.

Lilly is an equal opportunity employer and welcomes diverse candidates. We offer a comprehensive benefits package and opportunities for growth and development.



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