What are the responsibilities and job description for the Plasma Center Quality Control Specialist position at CSL Plasma?
About the Role
CSL Plasma is seeking a highly motivated and experienced Plasma Center Quality Control Specialist to join our team. As a Quality Control Specialist, you will be responsible for ensuring that our plasma collection operations are conducted in accordance with applicable laws, regulations, and company policies.
Key Responsibilities
- Conduct regular audits to monitor facility compliance with CSL procedures and policies, cGMP, OHSA, FDA, and other regulations.
- Develop center responses for deficiencies identified during audits.
- Collaborate with management to develop and implement corrective action plans.
- Ensure center records are accurate, complete, and compliant with regulatory requirements.
Your Skills and Experience
- Minimum 2 years' experience in a quality control or compliance-related role, preferably in a healthcare or pharmaceutical industry.
- Strong knowledge of regulatory requirements, including cGMP, OHSA, FDA, and other relevant regulations.
- Excellent communication and interpersonal skills, with the ability to build strong relationships with colleagues and external stakeholders.
Working Conditions
- Occasional travel required to attend meetings and training sessions.
- Ability to work in a fast-paced environment with multiple priorities and deadlines.
- Strong organizational and time management skills, with the ability to prioritize tasks effectively.
About Us
CSL Plasma is committed to making a positive impact on the lives of patients and donors. We are dedicated to providing high-quality products and services while maintaining the highest standards of safety and compliance.
CSL Plasma is seeking a highly motivated and experienced Plasma Center Quality Control Specialist to join our team. As a Quality Control Specialist, you will be responsible for ensuring that our plasma collection operations are conducted in accordance with applicable laws, regulations, and company policies.
Key Responsibilities
- Conduct regular audits to monitor facility compliance with CSL procedures and policies, cGMP, OHSA, FDA, and other regulations.
- Develop center responses for deficiencies identified during audits.
- Collaborate with management to develop and implement corrective action plans.
- Ensure center records are accurate, complete, and compliant with regulatory requirements.
Your Skills and Experience
- Minimum 2 years' experience in a quality control or compliance-related role, preferably in a healthcare or pharmaceutical industry.
- Strong knowledge of regulatory requirements, including cGMP, OHSA, FDA, and other relevant regulations.
- Excellent communication and interpersonal skills, with the ability to build strong relationships with colleagues and external stakeholders.
Working Conditions
- Occasional travel required to attend meetings and training sessions.
- Ability to work in a fast-paced environment with multiple priorities and deadlines.
- Strong organizational and time management skills, with the ability to prioritize tasks effectively.
About Us
CSL Plasma is committed to making a positive impact on the lives of patients and donors. We are dedicated to providing high-quality products and services while maintaining the highest standards of safety and compliance.
