Specialist II QA Operations

Employer
CSL Behring
Location
Kankakee, Illinois
Posted
Jul 13, 2021
Ref
R-139070
Hotbed
BioMidwest
Required Education
Bachelors Degree
Position Type
Full time

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

Responsibilities: • Under general supervision, maintains Quality Assurance System to ensure compliance with company and cGMP standards • Responsible for maintaining audit program, reviewing functional and release documentation and investigating deviations relevant to area of responsibility • Reviews lot release documentation and facilitates compliant release process for corresponding market • Responds to questions from authorities (Swissmedic, FDA, etc.) to ensure timely product release • Ensures standard operating procedures (SOP’s) stay current and align with corporate and regulatory requirements • Executes training/awareness related to GMP standards Qualifications: • University degree in a relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry) • 3+ years' GMP experience in pharmaceutical/biotech or other regulated industry • Knowledge of current Good Manufacturing Practices (cGMP) principles • Knowledge of FDA and EMA requirements Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.