Quality Technician 2

Location: Onsite in Alachua, FL

RTI Surgical is now Evergen!

This rebrand reflects our strategic evolution as a leading CDMO in regenerative medicine and comes at the end of a significant year for the business, including the successful acquisitions of Cook Biotech in IN. and Collagen Solutions, MN. Our new brand identity emphasizes our unique positioning as the only CDMO offering a comprehensive portfolio of allograft and xenograft biomaterials at scale.

About Evergen

Evergen (formally RTI Surgical) is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN., Eden Prairie and Glencoe, MN., Neunkirchen, DE., Glasgow, UK., and Marton, NZ.

Read more about this change and Evergen’s commitment to advancing regenerative medicine here: https://lnkd.in/eMSfVJkM

Job Responsibilities

• Provides quality support for the Quality Engineering functions such as manufacturing, sterility assurance, or supplier quality
• Performs investigations for product or supplier nonconformance and process noncompliance issues and documents exceptions appropriately in the Corrective Action / Preventative Action (CAPA) System
• Performs CAPA investigations using problem solving methodologies and a high attention to detail
• Participates in the review and disposition of non-conforming product or controlled process inputs including the Product Quality Review Board (PQRB), returns, and complaints
• Supports the review of validation documentation or new supplier qualification activities quickly and accurately in collaboration with engineers
• Performs audits of products or processes and documents the results appropriately
• Assists in the Change Management function including maintaining relevant work instructions, Standard Operations Procedures (SOPs), and other quality documentation
• Performs product acceptance testing, quality inspections, data entry, and data corrections quickly and efficiently
• May provide support for environmental monitoring investigations, documentation of quality inspections on controlled suppliers, or supports the Approved Supplier List monitoring activities
• Identifies and supports process improvement initiatives and implementation
• May support projects as a quality resource as assigned
• Other duties as assigned
  
  

Education

• High School diploma or equivalent
  
  

Experience

• 3-6 years of experience in quality assurance or quality control
• Additional education may substitute for experience requirement
  
  

Certification

• ASQ certification preferred
  
  

Skills

• Strong verbal and written communication
• Microsoft Office Suite, basic Excel
• Technical Writing
• Investigations
  
  

SAFETY

Physical Requirement

• Move or lift objects up to 25 pounds
• Frequent (>75%) stationary position (standing or sitting) while utilizing digital
• Frequent (>75%) fine manipulation using hands and fingers (typing, opening,writing, clicking, paper sorting, etc.)
  
  

Working Environment

Onsite: Office environment with assigned workstation