Today Lonza is a global leader in life sciences. We are more than 15,000 employees in more than 100 locations around the world. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
The Quality Control Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. Also participate in quality testing for ongoing customer stability studies. Provide on-time, high quality results to meet Manufacturing demands.
*** This position is an indefinite Second (2nd) shift role-- Ability to Work four ten hour shifts or five eight hour shifts-- Will cover a weekend workday****
Running test samples for Raw Material analyses via Compendial and in-house test methods.
Writing- Quality Records (Deviations, Corrective And Preventative Actions, Change Control) and Test Methods
Backup to Supervisor –independently making quality decisions with input
Projects – such as method transfers, new instruments, method qualifications
Perform other duties as assigned.
Bachelor or Associates Degree- preferred area of study: Microbiology, Biochemistry or Related Science Field
Advanced plus years of industry experience, preferably in a Good Manufacturing Practice (cGMP) environment
Shift is either 4/10hours or 5/8hours
Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries. Must comply with safety policies of the company and site.
Adherence to cGMPs is required at all times during the manufacture of APIs. All personnel own the quality of what they deliver and are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, process deviations, product defects and related actions.
Staying alert for duration of shift.
Being able to make quality decisions as to safety and task at hand.
Making quick decisions.
Maintain professional interactions with co-workers and superiors
Internal Number: R16134
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