Quality Technician II

Bioventus; Memphis (TN); On-site; USD 42,000 - 64,000; Full time

Job summary

Bioventus in Memphis seeks a quality inspector to visually and dimensionally inspect finished and in-process products, ensuring conformance to GMP and ISO13485 standards. You will review documentation, perform sterile product inspections, and ensure GDP compliance in all records.

The role uses calipers, micrometers, vision systems and timing gauges, with SAP and MS Office proficiency. ASQ/CQT CQPA and GD&T knowledge are preferred, supporting a culture of quality and patient safety.

Qualifications

• Two years of technical schooling or related experience in quality inspection.
• Experience with metrology tools and GMP/ISO13485 standards is preferred.
• ASQ certifications and GD&T knowledge are advantageous.

Responsibilities

• Inspects finished and in-process products to verify conformance to specs.
• Performs visual, dimensional, functional inspections and documentation.
• Reviews product documentation and maintains GDP records per GMP.
• Uses calipers, micrometers and advanced inspection equipment daily.
• Generates inspection reports and supports deviation investigations.

Skills

Detail oriented

Documentation

Microsoft Word

Microsoft Excel

SAP

Education

Two years of technical education in Mechanical or Industrial Engineering

Electronics Technician background

ASQ CQT or CQPA preferred

GD&T Certification preferred

Tools

Calipers

Micrometers

Vision measurement equipment

Timing Gauges

Pin Gauges

Thread Gauges

GDP documentation practices

Job description

Are you ready to work for a more active world?At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.Primarily responsibilities include inspection of finished and purchased products, raw materials and miscellaneous supplies by performing visual, dimensional, functional and documentation inspection per specified procedures or instructions within the framework of the FDA Good Manufacturing Practices (GMPs) and ISO 13485 standards.What you'll be doingPerforms routine visual inspection of partially complete, complete, or packaged products per procedure, specification, print, catalog, and/or visual standard.Performs inspection of product per procedure, specification or print using basic measuring equipment (caliper, micrometer, tape, height gage, etc.) and advanced inspection equipment (VMM, Optical Sensors, Timing Gauges, etc)Performs review of product documentation to verify acceptability per specification and GMP requirements.Conduct sterile product inspections.Completes documentation of inspection results and special studies when required.Uses inventory management software to perform work-in-process, inventory transactions and SPC data collection.Completes documentation using good documentation practices (GDP) and records deviation data in appropriate systems.Performs all related duties as defined by the Manager.Holds oneself and others accountable to conduct business in a manner compliant with Bioventus’ Code of Compliance and Ethics, policies and procedures and internal controls applicable to their role.Other duties as assignedWhat you'll bring to the tableTwo years education from technical school in Mechanical or Industrial Engineering, or Electronics Technician with 3 years related experience, or minimum of 5 years of relevant experience.Experience involving the use of Metrology inspection equipment is preferredPosition will require the use of calipers, micrometers, vision me, Timing Gauges, Pin Gauges, Thread Gauges, and other various inspection equipment.GD&T Certification is preferred.Certification from American Society of Quality (ASQ), such as a Certified Quality Technician (CQT) or Certified Quality Improvement Associate (CQPA) preferred.Proficiency in the use of Microsoft Word and Excel.Ability to use or learn SAP and other PC programs.Ability to analyze information and assess issues. Are you the top talent we are looking for?Apply now! Hit the “Apply” button to send us your resume and cover letter.Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.