What are the responsibilities and job description for the Senior Quality Specialist, Project QA, CQV position at CSL?
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
Education
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
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.
Education
- Degree in relevant scientific discipline, or related (Pharmacy, Chemistry, Biology, Biochemistry)
- 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.
- 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
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
Salary : $76,000 - $95,000