Process Quality Technician (MedTech)

Location: San Angelo, Texas, United States of America; onsite

Company

Johnson & Johnson MedTech develops innovative, less invasive, and personalized medical treatments at the intersection of biology and technology.

What you will do

• Investigate non-conformances and process failures, including NCR initiation, product control, corrective actions, and quality-system documentation.
• Create, revise, and periodically review SOPs, protocols, and controlled documents.
• Lead small Kaizen activities and apply root cause analysis methods such as 5M, 5 Whys, and Fishbone.
• Analyze quality data and recommend process, equipment, and system improvements.
• Train and guide manufacturing teams, provide day-to-day leadership to technicians and associates, and support special projects.
• Support internal and external audits, inspections, and compliance with safety, environmental, regulatory, QSR, GMP, and ISO requirements.

Requirements

• High School Diploma or equivalent.
• Strong computer skills, including Microsoft Word and Excel.
• Basic statistical and analytical problem-solving skills.
• Strong written and verbal communication skills with the ability to work independently and support multiple assignments.
• Ability to work rotating shifts, irregular hours, and some weekends as business needs require.

Nice to have

• Experience in QSR- or ISO-regulated medical device manufacturing.
• Experience with Minitab and formal problem-solving methodologies such as DMAIC, Fishbone, and 5 Whys.
• Experience preparing technical reports and presentations.
• Previous audit support or facilitator/lead experience.

Culture & Benefits

• Full-time employment with Johnson & Johnson MedTech.
• Regular schedule of Monday to Friday, 8 AM to 5 PM, with additional weekend work as needed.
• Inclusive work environment focused on individual dignity, diversity, and equal opportunity.