CSL Behring
- QC Analyst II
At a glance
Location: US-IL-Kankakee Map
Posted: 10/08/2021
Closing: 11/07/2021
Degree: 2 Year Degree
Type: Full-Time
Experience: Not Specified
Job description
About CSL

With operations in 35+ nations and ~27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL’s therapies. Seqirus is one of the largest influenza vaccine companies in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

Job Description


Position is in the QC Microbiology Lab/Environmental Monitoring (EM) Compliance Team

Collect, analyze, and report on EM data

Review EM data

Read EM plates and document results in logbooks and LIMS system

Subculture microbes for identification

Perform swabbing and sampling to support investigations

Gather and compile data from LIMS systems

Generate tables and graphs

Conduct Training

Perform change controls and Document revisions

Perform QC assessments for Environmental and Utility Monitoring deviations

Perform trending on environmental and utilities monitoring results

Support Environmental and Utility Monitoring sampling as needed

Follows Standard Operating Procedures (SOPs) and maintains compliance to current Good Manufacturing Practice (cGMP) regulatory guidelines


• Associate's degree in a relevant scientific discipline or equivalent vocational or technical training

• 3-5 years' related pharmaceutical experience including experience in a regulated environment

• Knowledge of cGMP standards

• Proficiency in Microsoft Office and QC systems

•Strong analytical, quantitative, and problem-solving skills.

•Capacity to work independently and ability to prioritize tasks and meet deadlines.

Preferred Qualifications

Experience in environmental sampling/monitoring

Experience in analytical laboratory data review

QC Analyst II