Demo

Quality Control Supervisor

public.client.lonza.display.name
Greenland, NH Full Time
POSTED ON 2/4/2025
AVAILABLE BEFORE 5/4/2025

Join Lonza, a global leader in life sciences, where we are dedicated to making a positive impact on the world by combining talent and innovative ideas. We empower our employees to take ownership of their careers, contributing to advancements that improve lives.

Position Overview

As a Quality Control Supervisor, you will be a key member of our Quality Control department, responsible for overseeing the testing of in-process and final product drug lots, supporting ongoing customer stability studies, and ensuring the safe and efficient execution of quality testing. Your role is vital for meeting manufacturing demands while fostering a culture of professionalism and safety within your team.

Shift Details

Night Shift : Monday-Friday, 8 : 30 pm - 5 : 00 am

Key Responsibilities

  • Ensure a safe working environment for all staff while executing their duties.
  • Cultivate a high level of professionalism and focus on product quality and patient safety.
  • Communicate safety procedures uniformly to all team members.
  • Handle non-routine assignments and recognize deviations from accepted practices.
  • Address advanced technical problems by analyzing various factors.
  • Schedule and plan routine quality testing activities.
  • Maintain safety standards for equipment and workplace areas.
  • Review assays, documentation, and quality systems.
  • Participate in relevant departmental meetings.
  • Independently lead projects to successful and timely completion.
  • Resolve personnel issues and enhance workplace dynamics through troubleshooting.
  • Lead continuous improvement initiatives and assist with various transfers and hiring processes.
  • Maintain a positive attitude and emotional stability in a team environment.
  • Ensure timely completion of assigned tasks, including punctual attendance for all shifts.
  • Make quality decisions independently or with managerial guidance.
  • Effectively lead meetings with direct reports.
  • Mentor and guide your team members.
  • Deliver constructive feedback and manage performance-related conversations.
  • Undertake complex and varied tasks as assigned.
  • Perform additional duties as required.

Key Requirements

  • Bachelor's degree in a scientific field, preferably Microbiology or Biochemistry.
  • M.S. or Ph.D. is preferred, with 2-5 years of experience in Quality Control in adherence to cGMP guidelines.
  • At least 2 years of direct supervisory experience is ideal.
  • Exceptional public speaking skills and meeting management capabilities.
  • Adept at data interpretation and assay troubleshooting within your expertise.
  • Proficient in workload prioritization and rapid problem-solving in unexpected situations.
  • Clear instruction and guidance for team analysts.
  • Strong capability in directing, controlling, and planning tasks and projects.
  • Excellent written and verbal communication skills.
  • A positive, proactive attitude with the ability to listen and follow through.
  • Strong influence and adaptability to meet business needs.
  • At Lonza, we understand that our success is tied to the well-being of our employees and the environment. We are committed to ethical practices and making substantial contributions to improving lives globally. If you are excited about working in a creative environment that allows you to tackle complex problems in life sciences, we encourage you to apply.

    Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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