
Associate Director, Project Quality, Vendor Qualification
Kankakee, ILJob$172–203K/yrSeen todaySeen in employer's feed today
Most applications go out cold — see where you stand first. No sign-up to start.
You apply on the employer's site, with no Olive account needed.
Watch jobs like this. New roles like this one near Kankakee, IL, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Requirements
Credentials this posting asks for.
Job overview
The Associate Director, Project Quality, Vendor Qualification provides Quality oversight for external supplier and vendor activities supporting CSL Behring’s Module 7/8 site expansion in Kankakee. The role ensures compliant end-to-end processes for GxP-related suppliers, service providers, and distributors, and leads a small team conducting external audits. It also serves as the site interface for supplier quality matters and supports supplier qualification, quality agreements, and audit planning.
Skills & qualifications
Skills
Qualifications
Full job description
Job Purpose:
The growing demand requires an expansion of CSL's manufacturing capacity. To support this growth, immunoglobulin (Ig) production activities—from plasma thawing through sterile filling—will be incorporated into the new Building at the CSL Kankakee (KAN) site to accommodate Ig production. The new fill-finish facility is part of the Ig manufacturing expansion, known as Module (M) 7/8 st CSL Behring Kankakee site.
This role will provide Quality oversight for the external supplier’s/vendor’s activities associated with the
Module 7/8 Site Expansion Project at the CSL Behring Kankakee site.
This position is responsible for ensuring that efficient, compliant, and end-to-end business processes are implemented and maintained for all GxP-related raw material suppliers, service providers, and distributors. The role also leads a small team of auditors responsible for conducting audits of external suppliers and service providers to ensure compliance with applicable regulatory and quality requirements.
Main Responsibilities and Accountabilities:
-
Implement strategic goals established by functional leadership.
-
Collaborate with External Supply Quality colleagues to manage overall supplier qualification auditing program including establishment of standardized auditor qualification requirements; on-site, remote or paper audit determination.
-
Through the identification and utilization of best-in-class practices, establish appropriate risk management tools, supplier and raw material monitoring concepts.
-
Serves as primary M7/8 site interface and point of communication of all supplier quality related matters or issues.
-
Attends local deviation review meetings and acts as quality liaison between Supplier and Site (M7/8 project scope) to assist deviation investigation processes.
-
Participates in change control process as required.
-
Performs quality systems audits of approved and/or potential suppliers of raw materials and components, service providers and distributors, for the M7/8 project.
-
May also perform M7/8 project site audits, as requested. Represents and articulates External Supplier Quality policies and procedures during regulatory audits.
-
Manages the activities of supplier quality agreements, global and local, which include writing, editing, reviewing, updating and routing the agreements for approvals between CSL New (M7/8) Manufacturing location, service providers and suppliers.
-
Supports the generation of fiscal year budgetary planning, ongoing forecasting for all external audits.
-
In collaboration with Global Sourcing, develops supportive and ongoing positive relationships with the external quality functions within CSL’s Critical Suppliers.
Qualifications:
-
Bachelor’s degree in relevant scientific discipline (biology, microbiology,chemistry, etc.); advanced degree preferred
-
10+ years’ experience in a GxP environment in the pharmaceutical industry.
-
Minimum 3 years’ experience in leading a team.
-
Thorough understanding of required regulations including but not limited to FDA, PIC/s and European regulation, Therapeutics Goods Administration, Canadian Health Authority, etc.
-
Strong industry knowledge (of CSL Behring’s process flow and the plasma business), and auditing knowledge (internal and external) experiences within the industry.
-
Must be comfortable working in a global, matrix organization.
Competencies:
-
Strong organizational skills. Managing diversity, time management and planning. Cross-cultural sensitivity, perseverance, written and verbal communication.
-
Demonstrated experience with directing others and delegation.
-
Managerial courage, decision quality, functional and technical skills.
-
Proficient in building consensus and escalating issues.
-
Excellent communication and organizational skills, as well as negotiation, influencing and collaboration skills. Fluent in English (written and spoken).
-
Demonstrated ability to work cross-functionally across internal and external stakeholders.
-
Effective presentation and meeting skills within all levels of the organization and with external colleagues and collaborators.
The expected base salary range for this position at hiring is $172,000 - $203,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed location as of the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.
About CSL Behring
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .
Our Benefits
For more information on CSL benefits visit How CSL Supports Your Well-being | CSL (https://www.cslbenefits.com/csl/candidates) .
You Belong at CSL
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging
Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .
R-295079
CSL makes all employment decisions without regard to race, color, religion, national origin, ancestry, age, sex, gender, pregnancy, disability, marital status, sexual orientation, gender identity, genetic information, military status, protected veteran status (specifically status as a disabled veteran, recently separated veteran, armed forces service medal veteran, or active duty wartime or campaign badge veteran) or other classification protected by applicable US federal, state or local law. CSL complies with all applicable employment laws, including but not limited to Title VII of the Civil Rights Act of 1964, the Americans with Disabilities Act, the Fair Labor Standards Act, and the Immigration Reform and Control Act. https://www.cslbehring.com/careers/eeo-statement
How this job compares
Set against the 5,028 open Quality Assurance jobs on Olive Jobs, counted November 6, 2026.
- Pay
- This posting$172–203K/yr
- Illinois median$87–132K/yr92 salary ranges
- US median$88–143K/yr2,275 salary ranges
This range's midpoint, $188K, is 62% above the Illinois median midpoint ($115K) — in the top quarter of Quality Assurance salary ranges in Illinois.
- Openings
- Olive Jobs lists 144 open Quality Assurance jobs in Illinois and 5,028 across the US. 3% of them nationwide are listed as remote or flexible.
- Hiring the most in Illinois
- CDM Smith8 open
- PCI Pharma Services7 open
- AbbVie6 open
- Experience
- This posting asks for at least 10 years of experience — more than three in four Quality Assurance postings that state a minimum ask for (median 5 years, across 3,859 postings).
- Education
- This posting asks for a bachelor's degree; 1,726 of the 5,028 open Quality Assurance jobs (34%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
Prepare for this role
You've read the whole posting — now see how you match it.