Sr. Quality Associate I, QA, Final Container Release

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

The Senior Quality Associate I, Quality Assurance may be assigned duties and responsibilities within Quality Assurance. Specific duties will depend on the assignment and may include; review of manufacturing or testing records, preparation or review of failure investigations, sampling/testing/data analysis, auditing, data analysis for stability, etc. The incumbent is an established and technically competent professional who develops and implements solutions to a variety of quality related objectives.

He/she may participate on teams or projects of varying scope and is often called upon by peers for his/her expertise or guidance. Demonstrates consistent application of technical knowledge and expertise, executes assignments of medium complexity, developing solutions for defined problems. The employee may be responsible for training other employees and is a fully qualified professional who requires minimal supervision.

Senior Quality Associate I, Quality Assurance

• Consults with management to develop and implement solutions for achieving quality related objectives.

• Assists in the effective deployment of divisional or departmental technical resources in pursuit of annual goals.

• Uses expertise to make independent decisions within defined areas of responsibility.

• Participates on multi-disciplined project teams. Also advances technical project proposals to senior management, following through to successful completion.

• Collects and analyzes data

• Prepares and reviews SOP revisions, technical reports in DCM, and Change Control Requests

• Demonstrated ability to make sound quality decisions with moderate guidance

• Prepares, reviews and/or approves Incident Tracking System entries and investigation reports.

• Demonstrates high levels of values and integrity.

• Follows cGMP and department safety practices.

• Other duties as assigned or as specified in the "Additional Responsibilities" section below may apply.

Senior Quality Associate I, Quality Assurance

In addition to the duties described above the Sr. Quality Associate I, Quality Assurance may also perform the following duties based upon the business unit to which he/she is assigned:

Responsibilities may include roles (such as author, reviewer, administrator or coordinator) in quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Responsible for representing Quality at business unit meetings, and project meetings.

Additional responsibilities may include preparation of release protocols and necessary certification for new market registration and license renewal. Support changing market requirements. Maintenance of release certificates of analysis, preparation of periodic RA reports, tracking batch release status including accepted, rejected, reprocessed, and reworked batches. Managing document revisions in support of change controls, projects, continuous improvement initiatives, etc. Support IT projects related to batch release.

Assist with tracking media fills and personnel training within the department.

Senior Quality Associate I, Quality Assurance

Excellent communication skills (written and verbal). Has basic knowledge/understanding of domestic (i.e. Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines.

Knowledge of current products, product specifications, different market requirements and regulations is preferred. In addition, knowledge of SAP QM is highly preferred.

Senior Quality Associate I, Quality Assurance

BS/BA degree preferably in a STEM (Science, Technology, Engineering, and Mathematics) discipline with minimum of 5 years relevant experience, or equivalent combination of education and experience.

Work is performed in an office and a laboratory/manufacturing environment or warehouse. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to occasional extreme cold below 32
* in production areas. Exposure to electrical office and laboratory equipment. Personal protective equipment required such as protective eyewear, garments and gloves. Work is performed sitting or standing for 2-4 hours per day. Frequent hand movement of both hands with the…