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Technician- QC Bulk Manufacturing-FDE - United States  

Lilly (company)

Posted on : 10 April 2017

Project Description

Technician- QC Bulk Manufacturing-FDE
United States
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 39,000 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.

The Technician – QC - IAPI performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Technician – QC - IAPI also participates in second person verification (SPV) of analytical data, laboratory investigations, equipment calibrations and maintenance by executing well-defined protocols and procedures. The Technician – QC - IAPI identifies and communicates opportunities for improvement within the lab.

Sample Analysis and Reporting

  • Accurately and safely perform analytical test methods or related support activities as per procedures or protocols and reviews that results conform to standards
  • Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards, and GMP requirements
  • Recognizes when a deviation from procedures, etc has occurred and initiates an investigation
  • Verify (SPV) analytical data of other analysts within the lab as required
Continuous Improvement Initiatives
  • Identifies and communicates opportunities for improvement initiatives in daily work activities
  • Troubleshoot equipment and methods as required
Lab Operations
  • Training and mentoring others within lab, where applicable
  • Executes notification to management when required by procedures or standards
Routine Lab Activities
  • Perform routine equipment qualifications/calibrations or maintenance through execution of well-defined protocols
  • Participate in laboratory investigations
  • Associates degree (2 yr College degree) in a science field related to the lab in which they are placed (e.g., chemistry for chem. Labs or micro or biology for micro lab) or
  • High School Diploma/GED with 5+ years of demonstrated relevant experience in a GMP (analytical chemistry or microbiology) lab
  • 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.
  • Proficiency with computer systems including Microsoft Office products, LIMS, etc.
  • Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations
  • Ability to work in a highly regulated environment
  • Demonstrated strong math and documentation skills
  • Demonstrated strong oral and written communication and interpersonal interaction skills
  • Bachelor's Degree in chemistry or biology
  • Night shift 5:45 pm - 6 am on a 3-2-2-3 rotation
  • Must complete applicable ITP for a Technician – QC – IAPI
  • Tasks may require repetitive motion and standing for long periods of time
  • Must be able to lift at least 5 liters of liquid
  • May be required to provide 24 hour pager coverage
  • This position is not permanent. It is for a fixed duration of two years with potential to extend annually for up to 4 years.
  • 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.