About this role
<style type="text/css"> table.MiTabla { max-width: 1020px;!important </style> <table border="0" cellspacing="0" cellpadding="0"> <tbody> <tr> <td><img src="https://staticweb.grifols.com/documents/675849/2554718/SSFF_02_CLAYTON.jpg/4f428334-9cb2-1679-ffa2-c56b3cd1097b?t=1636640425916" alt="" align="top/"></td> </tr> <tr> <td> <p style="text-align:justify">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.</p> </td> </tr> <tr> <td><img src="https://staticweb.grifols.com/documents/675849/2554709/SuccesFactors_1020x93_jobposting_line_test.png/e2cffc87-a707-9e08-b5ef-081cae1f1ecf?t=1636640341637" width="100%"></td> </tr> </tbody> </table><div id="tor__flistingLayout_readOnlyDiv"> <div id="tor__flistingLayout_content"> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Shift</strong>: 1st - M-F 8:00am - 4:30pm</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Summary:</strong></span></p> <p><span style="font-family:arial, helvetica, sans-serif">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. </span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Primary Responsibilities:</strong></span></p> <p><span style="font-family:arial, helvetica, sans-serif"><em>Senior Quality Associate I, Quality Assurance</em></span></p> <ul style="list-style-type:disc"> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Consults with management to develop and implement solutions for achieving quality related objectives.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Assists in the effective deployment of divisional or departmental technical resources in pursuit of annual goals.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Uses expertise to make independent decisions within defined areas of responsibility.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Participates on multi-disciplined project teams. Also advances technical project proposals to senior management, following through to successful completion.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Collects and analyzes data</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Prepares and reviews SOP revisions, technical reports in DCM, and Change Control Requests</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Demonstrated ability to make sound quality decisions with moderate guidance</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Prepares, reviews and/or approves Incident Tracking System entries and investigation reports.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Demonstrates high levels of values and integrity.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Follows cGMP and department safety practices.</span></li> <li style="font-family:arial, helvetica, sans-serif"><span style="font-family:arial, helvetica, sans-serif">Other duties as assigned or as specified in the "Additional Responsibilities" section below may apply.</span></li> </ul> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Additional Responsibilities:</strong></span></p> <p><span style="font-family:arial, helvetica, sans-serif"><em>Senior Quality Associate I, Quality Assurance</em></span></p> <p><span style="font-family:arial, helvetica, sans-serif">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:</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif">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.</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif">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.</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Knowledge, Skills, & Abilities:</strong></span></p> <p><span style="font-family:arial, helvetica, sans-serif"><em>Senior Quality Associate I, Quality Assurance</em></span></p> <p><span style="font-family:arial, helvetica, sans-serif">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.</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif">Knowledge of current products, product specifications, different market requirements and regulations is preferred. In addition, knowledge of SAP QM is highly preferred.</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Requirements:</strong></span></p> <p><span style="font-family:arial, helvetica, sans-serif"><em>Senior Quality Associate I, Quality Assurance</em></span></p> <p><span style="font-family:arial, helvetica, sans-serif">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.</span></p> <p> </p> <p><span style="font-family:arial, helvetica, sans-serif"><strong>Occupational Demands:</strong></span></p> <p><span style="font-family:arial, helvetica, sans-serif">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 ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Occasionally walks, bends and twists neck and waist, may reach above or below shoulder height. Frequent foot movements. Color perception/discrimination and near vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Performs tasks by following a set of written or oral instructions/procedures.</span></p> <p> </p> </div> </div><p style="margin-bottom:11.0px"> </p> <p style="margin-bottom:11.0px"><span style="font-size:11.0pt"><span style="font-family:Calibri, sans-serif">Third Party Agency and Recruiter Notice:</span></span></p> <p style="margin-bottom:11.0px"><span style="font-size:11.0pt"><span style="font-family:Calibri, sans-serif">Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.</span></span></p> <p style="margin-bottom:11.0px"> </p> <p style="margin-bottom:11.0px"><strong><span style="font-size:11.0pt"><span style="font-family:Calibri, sans-serif">Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.</span></span></strong></p> <p> </p> <p><img src="https://staticweb.grifols.com/documents/675849/2554709/SuccesFactors_1020x93_jobposting_line_test.png/e2cffc87-a707-9e08-b5ef-081cae1f1ecf?t=1636640341637" width="100%"></p> <p><strong>Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton</strong> </p> <p> </p> <p><a href="https://www.grifols.com/en/what-we-do" target="_blank" rel="noopener">Learn more about Grifols</a></p> <p> </p>