Team Lead - Lebanon, United States - Lilly

    Lilly
    Lilly Lebanon, United States

    Found in: Talent US C2 - 1 week ago

    Default job background
    Full time
    Description

    We're looking for people who are determined to make life better for people around the world.

    Organization Overview:

    At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

    Position Description:

    The QC Team Lead manages the day-to-day activities of QC analytical staff. Plans work for the group to respond to changing priorities. Maintains a safe, orderly, and compliant work area according to company safety standards and cGMP regulations.

    Key Objectives/Deliverables:

  • Manage the day-to-day activities of the assigned laboratory group.
  • Assign and monitor laboratory workload of routine and non-routine analyses by appropriate chemical, biochemical, and microbiological test methods. Performs assays as needed.
  • Plan and organize analytical projects required to achieve group and corporate objectives.
  • Evaluate, coach, and manage personnel performance. Set group objectives with mgt.
  • Build a strong, responsive team that is reliable, responsive, and flexible to shifting demands.
  • Work independently but ensure communication of critical information upward with buy-in from senior management for key decision-making.
  • Take initiative to make things better for the company, be aggressive with your work and assertive in your interactions, lead by example and build collaborative relationships.
  • Be a technical resource for QC.
  • Serve as a technical expert on the methods performed in the group and the results obtained.
  • Use scientific expertise to aid coworkers for troubleshooting, laboratory investigations and problem resolution. Implement process improvements with management.
  • Assure adherence of acceptable cGMP practices by staff during execution of all work tasks.
  • Compile and analyze data, prepare graphs, and write SOPs/reports. Conduct document reviews.
  • Review test results for conformance with specifications and effective documents.
  • Evaluate data to detect product or method-related trends. Write periodic trend summaries.
  • Basic Requirements:

  • Bachelor's degree in a related science (prefer Biology, Chemistry, Bio Chem)
  • 1+ year of previous supervisory experience in a QC lab
  • Additional Preferences:

  • Demonstrated strong problem solving and analytical troubleshooting skills.
  • Understanding of statistical tools and analysis.
  • Excellent interpersonal skills and networking skills.
  • Strong computer skills
  • Ability to organize and prioritize multiple tasks.
  • Demonstrated strong written and verbal communication skills.
  • Excellent working knowledge of cGMP regulations for QC laboratory applications is required.
  • Excellent teamwork and communication skills. Attentive to detail.
  • Ability to take initiative, to be assertive, to lead by example and to build relationships.
  • 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.

    Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.

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