Job Summary

INTEGRA Biosciences Corporation is an industry leader of innovative liquid handling products for the medical diagnostics, pharmaceutical, biotech, and food industries. The Quality Engineer is responsible for ensuring customer satisfaction by establishing procedures, monitoring process input and output capabilities, and leading continuous improvement activities. Coordinates and documents key quality department activities, including ISO maintenance, preventative and corrective actions, and lead continuous improvement activities.   This is a full-time, on-site position in Hudson, NH.

Primary Responsibilities

• Assist in developing, implementing, and maintaining an ISO quality management system 
• Assist in the internal audit program, documenting findings and following up on corrective/preventive actions
• Facilitate and lead corrective/preventive action reviews and other company improvement programs
• Identify potentials for product quality improvements and drive the improvement efforts
• Assist with the investigation and disposition of nonconforming material (MRB)
• Participate as a Quality representative on new product development teams
• Perform first-article inspections
• Develop quality measuring and reporting systems and implement quality improvement programs.
• Develop work instructions for relevant job tasks associated with products, processes, and testing requirements
• Compile and write training material and conduct training sessions on quality control activities
• Lead continuous improvement initiatives to improve quality and efficiency and reduce scrap

Qualifications and Requirements

• Associate or bachelor's degree in a related field
• One to five years of experience working in Quality management
• TPECS Certified in Quality Management Systems and System Auditing
• Experience in a manufacturing environment with quality systems such as ISO 9001 and ISO 13485
• Experience working with data and statistical analysis software
• Ability to problem solve and facilitate root cause analysis and corrective action
• Multi-task and handle multiple problems without routine management supervision
• Ability to use standard measuring equipment and assess equipment requirements to best fit the quality plan 
• Demonstrates the ability to work effectively with cross-functional work groups, including suppliers, customers, and associates, with both verbal and written communication.
• Strong problem-solving and analytical skills
• Experience with Microsoft Office products and statistical programs
• Must be fluent in English 

This job description is not an exhaustive list of all functions that the employee may be required to perform, and the employee may be required to perform additional functions. The company reserves the right to revise the job description at any time. The employee must be able to perform the position's primary functions satisfactorily and, if requested, reasonable accommodations may be made to enable employees with disabilities to perform the primary functions of their job, absent undue hardship.

INTEGRA Biosciences US is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, gender, national origin, disability, protected Veteran status, uniform service, sexual orientation, gender identity, gender expression, genetic information, or any other characteristic protected by law