Senior Quality Specialist, Project QA, CQV
CSL Kankakee, Illinois, United States · $76K–$95K/yr
Biotechnology Research · 10,001+ employees
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About the role
This role provides quality oversight for commissioning and qualification activities associated with the M 7/8 site expansion project. Responsibilities include ensuring GMP-compliant planning, reviewing CQV documentation, and supporting regulatory inspections and quality systems.
What they look for
Requirements
Candidates must hold a degree in a relevant scientific discipline and possess at least 5 years of experience in quality or GMP within the pharmaceutical or biotech industry. Strong knowledge of GxP, FDA, and EU regulatory guidelines is required.
Full description
The growing demand for an expanding production line 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 under construction 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.
This role will provide Quality oversight for the Commissioning and Qualification activities associated with the M 7/8 Site Expansion Project at the CSL Behring Kankakee site.
Responsibilities:
- Ensuring GMP-compliant planning and implementation of M7/8
- Maintains GMP-related quality systems including standard operating procedures (SOPs) and supportive systems to ensure cGMP compliance.
- Reviews and approves standards and procedures governing CQV quality systems and processes. Supports document management, change control, deviation handling, and supplier qualification.
- Supports all regulatory inspections, self-inspections and customer audits.
- Supports local & global change requests related to CQV activities
- Reviews and approves all CQV documents that include but are not limited to risk assessments, URSs, CQV protocols and reports.
Qualifications:
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 GxP, 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.
- Engineering experience desirable.
Competencies
- Knowledge of GMP, FDA, EU and other relevant GxP regulations
- Effective communication skills
- Good organizational and interpersonal skills
- Collaborate effectively with internal and external employees and
- stakeholders
The expected base salary range for this position at hiring is $76,000 - $95,000. 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.
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.
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