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Lead Chemical Operator - Peptide Synthesis

Job Overview

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Employment Type

Full-time
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Compensation

Hourly
Range $25.96 - $41.25
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Work Schedule

Rotating Shifts
Flexible
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Benefits

Health Insurance
Dental Insurance
Vision Insurance
Retirement Plan
Paid Time Off
Employee assistance program
Fitness benefits

Job Description

Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana, committed to uniting caring with discovery to improve life for people worldwide. With a rich history of innovation and dedication to advancing medical science, Lilly focuses on discovering and delivering life-changing medicines to patients globally. The company values putting people first and strives to foster a supportive and inclusive work environment through philanthropy, volunteerism, and employee resource groups. With employees working across various countries, Lilly emphasizes collaboration, ingenuity, and resilience to tackle complex healthcare challenges.

Currently, Lilly is undertaking its largest investment in manufacturing capacity by... Show More

Job Requirements

  • High school diploma or equivalent
  • authorized to work in the United States full-time without sponsorship
  • completion of post offer exam or work simulation if applicable
  • 3+ years chemical processing or comparable manufacturing experience

Job Qualifications

  • High school diploma or equivalent
  • 3+ years chemical processing or comparable manufacturing experience
  • knowledge of FDA guidelines and cGMP requirements
  • experience in pharmaceutical manufacturing with PSM-regulated hazardous chemicals preferred
  • previous facility or area start-up experience preferred
  • ability to lead and prioritize work independently
  • strong organizational and multitasking skills
  • understanding of lean manufacturing principles
  • ability to understand technical nomenclature and mathematical formulas
  • physical capability to handle manual material handling, bend, reach, stretch, climb ladders, and stand for long periods

Job Duties

  • Maintain compliance with all regulatory requirements at all times
  • support the execution of the production plan for the site
  • carry out daily monitoring testing and cleaning duties to ensure equipment and systems are maintained properly
  • enter Trackwise events and participate in and lead CAPA investigations
  • troubleshoot and diagnose process problems and take actions to minimize deviations or site impact
  • understand and apply health, safety, and environmental standards to execute GMP duties
  • monitor and collect data on equipment use and performance to anticipate potential problems
  • collaborate with maintenance and technical support to address utility supply upsets or equipment failure
  • communicate operational status and issues to other shifts during handover
  • actively participate in safety audits, procedure coordination, housekeeping, and improvement projects
  • be trained and qualified on all specified unit operations
  • identify and escalate concerns through formal and informal channels
  • adhere to cGMP practices, safety standards, hygiene, and housekeeping requirements
  • effectively communicate electronically, verbally, and in writing
  • demonstrate basic computer skills including desktop software usage

Job Qualifications

Experience

Mid Level (3-7 years)


Job Location

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