Want to know if you’re a fit? Upload your resume and let our AI show you.
Skills
Analysis Skillsunmatched
Asepsisunmatched
Capital Projectunmatched
Change Controlunmatched
Clinical Supportunmatched
Communication Skillsunmatched
Conflict Resolutionunmatched
Consultingunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Cross-Functionalunmatched
Detail Orientedunmatched
Drug Productsunmatched
Facilities Engineeringunmatched
GMP (Good Manufacturing Practices)unmatched
Gene Therapyunmatched
High Throughputunmatched
Laboratory Managementunmatched
Laboratory Operationsunmatched
Manufacturingunmatched
Manufacturing Operationsunmatched
Materials Managementunmatched
Operational Supportunmatched
Pest Controlunmatched
Problem Solving Skillsunmatched
Quality Assuranceunmatched
Quality Engineeringunmatched
Riskunmatched
Risk Analysisunmatched
Root Cause Analysisunmatched
Software Testingunmatched
Team Playerunmatched
Testingunmatched
Time Managementunmatched
Validation Planunmatched
Description
Job Description:
The Quality Engineering and Validation Consultant is recognized as an expert internally in the principles and application of quality assurance and compliance. This position coordinates GMP activities in support of clinical and commercial Drug Product manufacture. This position reports to Associate Director GMP Quality - Cell & Gene. This is an onsite Monday through Friday position. Responsibilities:
As part of the VCGT GMP Operational Quality group primarily responsible with providing quality oversight and support to Vertex Cell and Gene Therapy operations and capital projects in the following key areas/activities; support of manufacturing operations across all phases of development and commercial, support of validation, analytical laboratory, materials management, and facility/engineering groups.
Provide QA support of change controls, validation protocols, risk assessments, GMP investigations and CAPAs.
Responsible for identifying risks and communicating gaps for GMP process/systems
Provide Quality oversight and review of calibrations, PMs, eCRs, work orders and laboratory operations via instrument qualifications
Review and approval of trending programs (equipment, facility, utilities, etc.)
Support EM and Routine testing of facilities and utilities and control programs (Client/EMS, pest control, etc.)
Requirements:
Experience providing QA support and oversight of GMP manufacturing operations and capital projects
Aseptic processing
Experience successfully leading event investigations, Root Cause Analysis and CAPA
Experience with network-based applications such as Veeva, Nuvolo, Viewlinc
Master's degree with 3-5 years of relevant work experience, or bachelor's degree in engineering, scientific or allied health field with minimum 8 years of relevant work experience, or relevant comparable background.
Key Leadership Skills:
Collaboration / Teamwork / Conflict Management
Results Driver
Key Knowledge/ Skills and Competencies
The ability to thrive in a high throughput environment
Foster cross-departmental collaboration within project teams to ensure alignment and timely resolution of issues.
Ability to independently collaborate on cross-functional teams and represent the Quality unit
Ability to communicate effectively across all organizational levels
Critical Thinking / Problem Solving
Ability to evaluate quality matters and make decisions utilizing risk-based approach