Axogen
Director, Quality Assurance
Axogen, Vandalia, Ohio, United States, 45377
Axogen is hiring for a QA Director in Vandalia, OH!
Job Summary of the Director, Quality Assurance
The Director, Quality Assurance will be a key member of the AxoGen Leadership team with responsibility for establishing and administering all Quality functions related to cGXX (cGMP, QSR and cGTP) operations. The Director, Quality Assurance will provide quality oversight and support AxoGen’s manufacturing, processing, testing and product distribution functions. The position requires domestic and international travel, primarily to AxoGen locations to ensure compliance with domestic and international regulations.
Requirements of the Director, Quality Assurance
BA, MS or PhD with at least 10 years’ experience in a quality assurance or related role in the biologics or pharmaceutical industry is required
Demonstrated knowledge of cGXXs and relevant regulatory guidelines in the US and OUS.
Familiarity with ISO 13485 requirements for the design and manufacture of medical devices.
Experience at all phases of development, including commercialization.
Experience in leading external regulatory audits
Demonstrate experience in successful hiring and management of a quality or related organization/group.
Excellent oral and written communication skills
Excellent interpersonal and team-building skills
Ability to work independently, analyze and work with attention to detail, process and prioritize sensitive information and problem solve
Ability to exercise creativity and judgment
Experience with human tissue products or implantable medical devices is desirable
Experience with quality functions for biologics is required
Experience with Six Sigma and/or Lean Manufacturing desirable complex
Familiar with preparation of and guidelines for Chemistry, Manufacturing, and Controls (Module 3) worldwide regulatory submissions desirable.
Responsibilities of the Director, Quality Assurance
The specific duties of the Director, Quality Assurance include but are not limited to:
Establishes and administers AxoGen’s Quality Management System
Oversees all quality functions related to human tissue products, biologic products and medical devices.
Ensures compliance with relevant domestic and international quality requirements
Provides guidance on and administer process validation activities
Performs risk assessments and leads investigations to address quality issues
Performs release and disposition functions; manages and controls cGXX-manufactured intermediates and products; works with AxoGen Operations, Clinical and Translation Science staff as required
Represents AxoGen during external audits and inspections and ensures pre-approval inspection readiness
Participates in vendor selection, assessment and qualification
Works with internal and external technical teams (process, analytical, formulation development, quality control)
Recruits, develops, and manages the Quality Assurance department as the company’s pipeline and development activities grow
Develops budget for Quality Assurance department
Axogen is a dynamic environment and each employee may be asked to assist in work areas outside of their usual duties. This is an expectation of every employee and it allows for future growth opportunities.
As a key and senior member of the Axogen Leadership team, the Director is expected to participate in operational and strategic discussions that impact the entire organization.
Other duties as assigned Experience and judgment to plan and accomplish goals. Performs a variety of tasks. Leads and directs the work of others.
Location
913 Industrial Drive Place, Vandalia, OH 45377
#J-18808-Ljbffr
Job Summary of the Director, Quality Assurance
The Director, Quality Assurance will be a key member of the AxoGen Leadership team with responsibility for establishing and administering all Quality functions related to cGXX (cGMP, QSR and cGTP) operations. The Director, Quality Assurance will provide quality oversight and support AxoGen’s manufacturing, processing, testing and product distribution functions. The position requires domestic and international travel, primarily to AxoGen locations to ensure compliance with domestic and international regulations.
Requirements of the Director, Quality Assurance
BA, MS or PhD with at least 10 years’ experience in a quality assurance or related role in the biologics or pharmaceutical industry is required
Demonstrated knowledge of cGXXs and relevant regulatory guidelines in the US and OUS.
Familiarity with ISO 13485 requirements for the design and manufacture of medical devices.
Experience at all phases of development, including commercialization.
Experience in leading external regulatory audits
Demonstrate experience in successful hiring and management of a quality or related organization/group.
Excellent oral and written communication skills
Excellent interpersonal and team-building skills
Ability to work independently, analyze and work with attention to detail, process and prioritize sensitive information and problem solve
Ability to exercise creativity and judgment
Experience with human tissue products or implantable medical devices is desirable
Experience with quality functions for biologics is required
Experience with Six Sigma and/or Lean Manufacturing desirable complex
Familiar with preparation of and guidelines for Chemistry, Manufacturing, and Controls (Module 3) worldwide regulatory submissions desirable.
Responsibilities of the Director, Quality Assurance
The specific duties of the Director, Quality Assurance include but are not limited to:
Establishes and administers AxoGen’s Quality Management System
Oversees all quality functions related to human tissue products, biologic products and medical devices.
Ensures compliance with relevant domestic and international quality requirements
Provides guidance on and administer process validation activities
Performs risk assessments and leads investigations to address quality issues
Performs release and disposition functions; manages and controls cGXX-manufactured intermediates and products; works with AxoGen Operations, Clinical and Translation Science staff as required
Represents AxoGen during external audits and inspections and ensures pre-approval inspection readiness
Participates in vendor selection, assessment and qualification
Works with internal and external technical teams (process, analytical, formulation development, quality control)
Recruits, develops, and manages the Quality Assurance department as the company’s pipeline and development activities grow
Develops budget for Quality Assurance department
Axogen is a dynamic environment and each employee may be asked to assist in work areas outside of their usual duties. This is an expectation of every employee and it allows for future growth opportunities.
As a key and senior member of the Axogen Leadership team, the Director is expected to participate in operational and strategic discussions that impact the entire organization.
Other duties as assigned Experience and judgment to plan and accomplish goals. Performs a variety of tasks. Leads and directs the work of others.
Location
913 Industrial Drive Place, Vandalia, OH 45377
#J-18808-Ljbffr