Principal Quality Associate
Location : NC-Clayton, US
Contract Type : Regular Full-Time
Area : TECHNICAL
Shift : Day - Monday through Friday 8 : 00am-5 : 00pm
The incumbent will be assigned duties and responsibilities within Quality Assurance to support the QA Fraction II Business Unit which provides Quality oversight for the following GT products : IGIV-C, IGSC, IGIM-C, and IGCP. In this role the incumbent will interface with plant manufacturing and support groups to execute site quality systems. Specific duties may include serving as author, reviewer, administrator or coordinator for quality systems such as Change Control, Discrepancy Management (including deviations, Product Technical Complaints and CAPAs), Quarantine, Documentation, and Annual Product Reviews as well as providing Quality input for Validation projects, Regulatory submissions and audits. The incumbent will serve as a Fraction II product line representative and be responsible for representing Quality at project meetings. The incumbent is an established and technically competent professional who develops and provides solutions / is able to influence the direction of project / quality related objectives.
The incumbent may participate on teams or projects of varying scope and is often called upon by peers for their expertise or guidance / is recognized as an authority in multiple areas. The incumbent demonstrates consistent application of technical knowledge and expertise, executes assignments of medium to complex nature, developing solutions for defined technical problems. The employee may be responsible for training other employees and is a fully qualified professional who requires minimal supervision.
The incumbent must have a strong knowledge of cGMPs, the ability to perform independently, and the ability to solve moderate technical problems. Knowledge of routine and non-routine assays, test method development, test method validations, Stability, product characterization, and / or manufacturing processes is preferred. A proactive philosophy, attention to detail, and good human interaction skills are essential and must have been demonstrated in previous work. The incumbent should be able to prepare reports / presentations and be able to effectively communicate information to varying levels of management.
The incumbent should be able to actively participate on teams of varying complexity. The incumbent must be a professional with moderate to high technical competence. Incumbent must have good to excellent judgement, and investigative, analytical, and organizational skills. Desired computer skills include Excel, Word and SAP. Experience with plasma products, Immune Globulin products or other biological products is a plus.
Requirements :
Sr. Quality Associate I -M8 : BS / BA degree in STEM (Science, Technology, Engineering, and Mathematics) discipline required with minimum of 5 years relevant experience, or equivalent combination of education and experience.
Sr. Quality Associate II - M9 : BS / BA degree in STEM (Science, Technology, Engineering, and Mathematics) discipline required with minimum of 6 years relevant experience, or equivalent combination of education and experience
Principal Quality Associate - M10 : BS / BA degree in a STEM (Science, Technology, Engineering, and Mathematics) discipline required with minimum of 8 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
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.
Quality Associate • Clayton, NC, US