Join Our Team at Lonza
Lonza is a global leader in life sciences, impacting millions of lives around the world. We believe in the power of collaboration and innovation, and we're looking for talented individuals to help us continue making a difference. Here, you have the opportunity to take ownership of your career and contribute to groundbreaking scientific solutions.
Job Summary
As a Quality Control (QC) Supervisor, you will play a crucial role in supporting the production of in-process and final product drug lots. You will organize and plan quality testing for ongoing customer stability studies, ensuring timely and high-quality results to meet our manufacturing demands. Your role is pivotal in fostering a safe, professional work environment focused on product quality and patient safety.
Benefits of Working Night Shift
This position is scheduled from Monday to Friday, 8:30 PM to 5:00 AM, allowing for a structured night schedule that enhances work-life balance.
Key Responsibilities
Ensure a safe work environment for staff during their duties.
Create and promote a culture of disciplined execution and professionalism focused on product quality and patient safety.
Clearly communicate safety procedures and monitor adherence among all staff members.
Address complex technical problems and analyze situations involving multiple factors.
Schedule and plan routine quality control tasks effectively.
Maintain safety in both equipment and work areas for all employees.
Conduct assay documentation and quality system reviews.
Participate in department-related meetings to ensure alignment and communication.
Drive projects to timely completion with minimal supervision.
Resolve personnel and workplace conflicts, troubleshooting operational issues.
Lead operational excellence initiatives and assist in staff hiring and transfers.
Foster a positive and composed team environment.
Complete tasks in a timely manner and adhere to assigned shifts.
Make informed decisions independently and with managerial guidance.
Maintain control during team meetings and effectively mentor direct reports.
Deliver necessary feedback and address performance-related issues directly.
Perform additional complex tasks as needed.
Key Requirements
Bachelor's degree in a scientific field, preferably Microbiology or Biochemistry.
M.S./Ph.D. degree is preferred, along with 2-5+ years of experience in Quality Control adhering to cGMPs.
Ideally possess 2+ years of supervisory experience.
Exhibit strong public speaking skills and effective meeting management.
Demonstrate proficiency in data interpretation and troubleshooting within your area of expertise.
Ability to prioritize and adapt workloads in response to changing situations.
Effectively communicate instructions and expectations to team members.
Manage tasks and projects with confidence and clarity.
Outstanding written and verbal communication skills.
Maintain a positive, approachable demeanor and actively listen to team members.
Possess flexibility to adapt to the evolving needs of the business.
At Lonza, we are committed to ethical practices, safeguarding our people and the environment. Join us, to not only find professional fulfillment but also contribute to solutions that positively impact health and lives globally.
Lonza is an equal opportunity employer. We welcome all qualified applicants without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability status, veteran status, or any other characteristic protected by law.
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