Dexian

Compensation

Full Description

Job Title: Quality Assurance Project Manager (Pharma) Location: Chesterfield MO(HYBRID) Pay Rate – $60 - 70/hr On W2 Duration – 8 Months Job Summary: This position serves as a critical liaison between quality systems and breeding operations, ensuring seamless integration and optimization of quality management tools across research and development structures. The role demands a strategic thinker who can balance technical system administration with user support and training, while maintaining compliance with regulatory requirements. This individual will be responsible for managing multiple quality platforms, developing training materials, troubleshooting system issues, and ensuring data integrity across interconnected dashboards and tools. The position requires close collaboration with breeding organizations, laboratories, field solutions teams, and plant biotechnology groups to maintain robust quality governance and facilitate informed decision-making through accurate reporting and analytics. Responsibilities: • Serve as K-User for GIMS, managing user profiles, coordinating IT tickets for new profile requests, and providing troubleshooting support to breeding organizations • Maintain and update GIMS training manuals and conduct training sessions for quality representatives across breeding areas and modules • Administer myDoc system as K-User, including library creation, review, updates, and settings management • Coordinate myDoc keyword management and restructuring initiatives based on organizational requirements • Oversee quality governance document lifecycle management within the QSC Hub role • Configure and maintain Training and Competencies tool settings, including business and administrative access, areas, and locations • Create, translate, and update training documentation and conduct user training sessions across multiple quality platforms • Manage Quality KPI Dashboard connections with myLearning, myDoc, GIMS, Intelex, MOC, and assessment tools • Collect organizational feedback to optimize dashboard functionality and communicate requirements to developers • Complete development and implementation of the Framework Assessment Dashboard and ensure integration with Quality KPI Dashboard • Co-lead biennial FSMA FDA Food Safety Modernization reviews with Regulatory Affairs in October • Ensure proper completion of site assessment forms and support Site Responsible Representatives with regulatory inquiries • Maintain FDA registration compliance for facilities manufacturing, processing, packing, or holding food products for human or animal consumption • Guarantee connectivity and data flow between breeding operations and other R&D structures including laboratories, field solutions, and plant biotechnology teams Skills: • Advanced proficiency in quality management systems and database administration • Strong technical aptitude for learning and managing multiple software platforms simultaneously • Excellent training and presentation skills with ability to create clear documentation and instructional materials • Superior troubleshooting and problem-solving capabilities • Outstanding communication skills for liaising between technical teams and end users • Project management abilities to coordinate system implementations and rollouts • Analytical skills for dashboard development and data integrity verification • Knowledge of regulatory compliance requirements, particularly FDA regulations • Ability to translate complex technical concepts into user-friendly training materials • Strong organizational skills to manage multiple systems and stakeholder relationships concurrently Experience: • Previous experience in quality assurance or quality management roles • Demonstrated background in system administration or technical support • Experience developing and delivering training programs • Prior work with document management and quality management systems • Background in regulatory compliance or working with regulatory affairs teams • Experience supporting research and development or breeding operations preferred Qualifications: • Understanding of FDA Food Safety Modernization Act requirements • Knowledge of quality governance frameworks and assessment methodologies • Familiarity with GxP principles and quality system regulations Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit https://dexian.com/ to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.