Top 15 Quality manager Jobs in Kankakee Il

Manager, Project Quality Validation
CSL Behring —Kankakee, IL
- $91,000 - $120,000 a year
- Full-time
- 5 years
- English
- Office
Program Manager, Quality Specification
VanDrunen Farms —Momence, IL
- $85,000 - $95,000 a year
- Full-time
- Hybrid work
- 5 years
- Bachelor's degree
- Organizational skills
- Paid holidays
- Health insurance
Quick Apply
1d
Project Quality Manager
Exyte GmbH —Kankakee, IL
- Engineering
- 11+ years
- Electrical experience
OSM/MEP Manager (Construction Manager) - QC/W
Exyte GmbH —Kankakee, IL
- Microsoft Excel
- Construction site
- 11+ years

More jobs to discover

Find similar jobs that you might be interested in.

Program Manager, Quality Specification
VanDrunen Farms —Momence, IL
Background in food manufacturing or dietary supplement quality assurance, with CPG experience preferred. Five or more years of quality assurance experience,…
$85,000 - $95,000 a year
Quick Apply
1d
Standardized Patient Program Manager
The University of Chicago —Chicago, IL
Conducts research and development of curriculum, models, and best practices in the field of education. Pursue continued professional development in the field of…
$70,000 - $95,000 a year
14d

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Director of Quality Management
Select Specialty Hospital - Southeast Ohio —Newark, OH
Registered Nurse with valid state license. Completing monthly quality related data entry, analysis and reporting. Bachelors or masters in nursing preferred.
Quick Apply
12d
Quality Control Supervisor
Monster Digital —Columbus, OH
Previous experience leading quality in a manufacturing/production environment. Provide quality inspection in every step of production and oversee the auditors…
$48,723.21 - $58,677.41 a year
Quick Apply

Show more jobs in cities nearby

I want to receive the latest job alert for quality manager in kankakee il

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Manager, Project Quality Validation

CSL Behring -
Kankakee, IL

Apply Now

Job Details

Full-time
$91,000 - $120,000 a year

Qualifications

Biotechnology
Drug regulation
Manufacturing facility experience
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
QA/QC
Regulatory/legal compliance standards in production
Cleanroom experience
Biomedical regulatory compliance
Commissioning phase involvement
Stakeholder relationship building
FDA regulations
Pharmaceutical manufacturing facility experience

Full Job Description

Entity: CSL Behring

Job Category: Quality

Job Family: Quality Assurance

Job Type: Full Time

Location: Kankakee, Illinois, United States

Employer Reference: R-285852

Job Description

Job Purpose:

The growing demand for Privigen and Hizentra 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 45 at the CSL Kankakee (KAN) site to accommodate ZAPP Ig production. The new fill-finish facility is part of the Ig manufacturing expansion, known as Module (M) 7/8 at the CSL Behring Kankakee site.

This role will provide Quality oversight for the Commissioning and Qualification activities (C & Q). Partnering closely with colleagues in Project Quality, KAN Site Quality, Global Engineering, and TechOps across multiple manufacturing sites to ensure consistent application of quality principles, systems, and documentation standards.

The incumbent will focus on driving a standardized approach across projects, ensuring alignment in processes, documentation, and execution.

Responsible for building and maintaining strong collaborative relationships across all levels of the organization and with external contractors.

Responsibilities & Accountabilities:

Ensure GMP-compliant planning and implementation of validation related project tasks.
Maintain quality systems including standard operating procedures (SOPs) and supportive systems to ensure cGMP compliance.
Review and approve standards and procedures governing quality systems and processes. Supports document management, change control, deviation handling, relevant to C&Q.
Support all regulatory inspections, self-inspections, internal audits and customer audits
Collaborate cross-functionally and communicate best practices
Provide Quality Oversight of the GMP-compliant realization of CAPEX and OPEX projects
Provide technical advice on qualification and validation issues/concepts.
Actively participate in problem solving and identifying opportunities for improvement to optimize validation activities.
Reviews and approves equipment, utilities, facilities documentation for qualification and validation activities (i.e. Protocols, Reports, Revalidations etc.)
Reviews and approves validation governance documentation including procedures, templates, project plans, risk assessments and validation master plan for site processes and support with the delivery of global approaches.
Actively maintain current knowledge relating to equipment qualification and validation activities. Information will be gained through regulatory, industry, and company sources.
Promote the education and implementation of the relevant regulatory requirements including the FDA, PIC/S, EMA and other industry regulations and guidelines (PDA, ICH etc.)

Education:

Degree in relevant scientific discipline, or related (Pharmacy, Chemistry, Biology, Biochemistry)

Experience:

5 years' experience in quality/GMP in the pharmaceutical/biotech industry
Demonstrates experience in quality assurance and regulatory compliance with FDA, TGA, EU, and other regulatory agency guidelines and in manufacturing of biologics
Experience in quality oversight of GMP-compliant commissioning and qualification of production facilities, equipment, and cleanrooms
Strong quality process knowledge
Experience in working in a matrix/global environment
Engineering experience desirable

Competencies:

Efficient and risk-based decision-making ability in a quality environment
Knowledge of GMP, FDA, EU and other relevant GxP regulations
Ability to influence others through clear, concise and effective communication
Good organizational and interpersonal skills
Collaborate effectively with internal and external colleagues and stakeholders
Experience in project-oriented working methods
Fluent English skills (spoken and written)

Working Conditions:

As defined in an office position. Primarily sitting and working on a computer.

Travel Requirements:

Potential travel required

The expected base salary range for this position at hiring is $91,000 - $120,000. 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.

Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable

#GTA

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.

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.

Apply Now

Refine Your Search

quality manager jobs in kankakee il

Manager, Project Quality Validation

Program Manager, Quality Specification

Project Quality Manager

OSM/MEP Manager (Construction Manager) - QC/W

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for quality manager in kankakee il

Explore jobs in more locations

Job Description

About CSL Behring

Our Benefits

You Belong at CSL

Equal Opportunity Employer

Job Seeker Tools

Employer Tools

Browse

Stay Connected