Manufacturing Process Technician

1 week ago

Durham, North Carolina, United States Lilly Full time

Overview:

At Lilly, we are dedicated to enhancing lives globally through innovative healthcare solutions.

Company Background:

  • Lilly is a prominent global healthcare organization headquartered in Indianapolis, Indiana, with a workforce of 35,000 dedicated employees. Our mission is to discover and deliver transformative medicines to those in need, while also fostering community engagement through philanthropy and volunteer initiatives.
  • For over 140 years, we have been at the forefront of medical advancements, with our research teams focused on developing new treatments to address significant health challenges. We leverage cutting-edge therapeutics, advanced technologies, and data analytics to enhance patient outcomes and the overall healthcare landscape.
  • We are currently in the process of establishing a state-of-the-art facility in Raleigh-Durham, North Carolina, aimed at manufacturing, assembling, and packaging parenteral drug products.

Benefits:

  • Comprehensive medical, dental, vision, and prescription coverage effective from day one.
  • Generous paid vacation policy starting at 120 hours annually, prorated based on start date.
  • Sign-on bonus of $3,000.

Key Responsibilities:

  • Support commissioning and qualification activities during the project phase to prepare formulation suites for operational readiness.
  • Execute daily operational tasks as directed by the shift lead or supervisor post-project phase.

Primary Objectives:

  • Ensure adherence to safety protocols and contribute to a secure working environment.
  • Follow standard operating procedures and Good Manufacturing Practices to maintain product quality.
  • Document process steps accurately using appropriate batch documentation systems.
  • Achieve and maintain qualifications for operating assigned process equipment.
  • Identify and implement opportunities for operational enhancements.
  • Monitor documentation and product quality proactively, ensuring all activities are properly recorded and issues reported.
  • Contribute to departmental goals focused on improving safety, reducing deviations, enhancing productivity, and ensuring training compliance.
  • Willingness to work 12-hour shifts and adapt to non-routine tasks while prioritizing safety and integrity.
  • Provide support for commissioning, qualification, and operational readiness during the project phase.
  • Assist site leadership in developing operational procedures and quality controls for the parenteral formulation area.

Basic Qualifications:

  • High School Diploma or equivalent.
  • Effective communication skills, both written and verbal.
  • Flexibility and strong problem-solving abilities.
  • Basic digital literacy required.
  • Ability to pass a fitness for duty physical examination.
  • Legally authorized to work in the United States without sponsorship.

Preferred Qualifications:

  • Familiarity with Good Manufacturing Practices (CGMPs).
  • Experience in pharmaceutical operations.
  • Background in compounding/formulation within a controlled environment.
  • Knowledge of lean manufacturing principles.
  • Certification in BioWork.

Additional Information:

  • Ability to wear required safety equipment.
  • Flexibility to work remotely during project phases with managerial approval.
  • Capability to work in controlled classified areas.

Lilly is an equal opportunity employer and values diversity in the workplace.

We are committed to supporting individuals with disabilities and ensuring equal opportunities in the hiring process.

#WeAreLilly

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