QA Manager

Job Description

Job Description

KEDPLASMA provides a friendly and rewarding working environment with frequent opportunities for cross-training and advancement.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status.

Please be advised that our organization participates in E-verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.

S. For more information on E-verify, please contact the Dept. of Homeland Security.

Kedrion Biopharma & KEDPLASMA offer a number of benefits to qualifying employees, including :

• Medical, vision and dental insurance
• Life and AD&D insurance
• Paid holidays
• PTO accrual
• and much more!

Please let us know if you would like further details regarding the benefits that we offer to our qualifying employees, and we would be glad to provide you with our full benefits guide, as well as answering any questions you may have!

Please note that salary ranges are calculated based off levels of : relevant experience, education and certifications.

Duties and Responsibilities :

1. QAM is responsible for oversight of all activities relating to product quality.

2. QAM should work in collaboration with Center Manager to assure product quality.

3. The QAM should coordinate, monitor, and facilitate all QA activities.

4. Ensure general understanding of all applicable state, federal regulations, industry and corporate policies.

5. Ensure that production personnel follows compliance of all Center activities with cGMP, Kedplasma DCOP’s (Donor Center Operating Procedures) and other Company standards and protocols to meet the regulatory requirements of the FDA, EMEA, Customer Specifications, and other regulatory bodies as required.

6. Ensure plasma release and shipments meet specifications and requirements as defined by customers and in DCOPs. When necessary, should have the authority to stop production and / or release of product.

7. Review and investigate final shipment release deviations including accurate labeling and documentation of shipments.

8. Determining that DCOP’s exist for all manufacturing procedures including, but not limited to, testing, and that DCOPs accurately describe and define the procedure, including a statement of what the procedure is intended to accomplish.