Company Profile
esrhealthcare.com.mysmartjobboard.com
Experience level: Associate Experience required: 3 Years Education level: Bachelor’s degree Job function: Engineering Industry: Logistics and Supply Chain Pay rate : View hourly payrate Total position: 3 Relocation assistance: No
This role is contract to hire and offers hybrid work model!
Job Summary/Description
This QA Computer System Validation Supervisor provides guidance to UPS Supply Chain Solutions (SCS) Information Technology (IT) department to maintain validation of warehouse or support systems utilized for healthcare applications. This role assesses systems being evaluated for use in healthcare applications, provides training and subject matter expertise to achieve/maintain validated status. The incumbent identifies systems requiring validation, escalates validation issues appropriately, and provides validation expertise. This position manages validation documents, determines applicable regulations, and reviews and approves testing of changes to validated systems.
The incumbent consults with internal groups (e.g., Operations, Business Development, IT, etc.) investigates and resolves healthcare issues to ensure compliance with rules and regulations. This position writes and revises Standard Operating Procedures (SOPs) and work instructions to ensure proper procedures are followed by Operations, IT or Order-to-Cash personnel. This role participates in information gathering and scheduling to prepare for internal and client audits. The incumbent assesses current SCS capabilities to determine SCS's ability to meet client requirements and proposed solutions. This position develops and revises change control procedures, training, and audits to ensure the maintenance of validation.
Job Duties
Writes, executes, and reviews validation protocols, generates validation reports, and performs corrective actions for deviations to provide subject matter expertise for SCS in validation matters
Reviews policies, procedures, and regulations with internal/external clients to determine specialized requirements and ensure compliance
Coordinates document and data control (e.g., numbering, version control, controlled copies, etc.) to ensure documentation and data are maintained in an orderly manner and meet quality standards
Leads validation personnel or projects, when assigned
Records information and observations from internal audits to support the preparation and distribution of internal audit reports
Establishes and maintains quality policies and programs within the IT area to ensure proper document and data control methods are utilized
Interfaces with client QA departments and attends sales presentations and business reviews to support the coordination of client activities
Interacts with internal auditors to discuss audit plans and findings
Ensures continued learning of new/existing regulatory requirements by the various regulatory bodies governing our healthcare industries
Participates in consultations with Corporate Legal to determine compliance implications of pending business
Ensures consistent and timely completion of compliance-base tasks as assigned including but not limited to NCs, CAPAs, Audit findings and Document Changes/Management
Follows up with clients after audits to identify issues and mutually acceptable solutions
Minimum Requirements
Bachelor's Degree (or internationally comparable degree) in Computer Science, Information Systems or related field – Preferred
Possesses knowledge of Supply Chain logistics
Experience in the Healthcare industry
Minimum of 3 years' computer system validation in a pharmaceutical/medical devices environment, including thorough knowledge of regulations and guidelines (21 CFR Part 11, 211, 820, and Annex 11), experience writing VMP, VSR, and IQ/OQ/PQ protocols, and SDLC methodologies (GAMP)?
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