Quality Reviewer / Day - III

Title: Quality Specialist-Level-1 Rate: $31/HR Location: Remote Qualifications: Quality Specialist-Level-1 Years of Experience : 3-5 Required Qualifications: 3-5 years of Quality, Operational, or technical experience within a Biotechnology, Pharmaceutical, or Device Industry environment. Quality Systems experience. Experience with data analytic tools (e.g. Spotfire, Qliksense, PowerBI, PowerApps) Must have strong Excel experience. Strong written and oral communication ability. Ability to work independently in a diverse environment. Advanced proficiency in Excel (pivot tables, handling large data sets, complex Excel functions, etc.) Experience working with relational databases (such as Access, etc.) or other quality management systems databases in the CGMP Pharma environment. Ability to lead virtual meetings and present to large groups and various levels of the organization. Education Requirements: Bachelor's degree in science, engineering, or related areas of study. Preferred Qualifications: Previous experience with SAP and or management of master data, specifically with supplier data management desired Supplier Quality Management (SQM) experience desired, including Approved Supplier List data management. • Note*: This is a 100% remote role. 40 hours/week, one (1) year assignment with the possibility of extension. Responsibilities: Works in an empowered, self-directed culture with independent decision-making in the planning, coordinating, and executing SQM activities. Review data entered by system users, perform data quality approvals, enforce and audit data for compliance with system and procedure requirements, and work with system users to address any identified data discrepancies. Perform data queries/ reports to meet customer needs and assist in system procedural updates, user training, and enhancements. Maintains an active dialog and communication with the Global SQM team to ensure progress and milestone success. Primarily responsible for supporting data quality governance and day-to-day support for the MMD supplier management system. Support other areas of the SQM as directed by Global SQM leads. Partner with various global and site organizations to achieve business goals. Proactively support and provide guidance relative to Quality Data Governance within the Supplier Quality and site-impacted space. Review and appropriately disposition data in the supplier management system. Support creating business processes, procedures, tools, and training to ensure accurate supplier data. Track and trend supplier master data quality and support visibility to applicable sites/global functions. Provide inputs into Community of Practice, Office Hours, and/or Knowledge networks across the Supplier Quality community related to assigned areas. Review and respond to inquiries regarding system management. Escalate potential risk to Global SQM lead. If interested; kindly share your resume with answers: Q1-How many years of exp in a Biotechnology, Pharmaceutical, or Medical Device Industry environment. Q2: How many years of exp in Supplier Quality Management (SQM) experience, including Approved Supplier List data management. Q3: How many year of exp with SAP and or management of master data, specifically with supplier data management Q4: This is a fully remote position to work n Eastern time ; which city you are based at Apply Job!