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
Seniority level
Entry level
Employment type
Full-time
Job function
Quality Assurance
Industries
Biotechnology Research
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