American Society for Quality (ASQ), Certified Quality Engineer (CQE), Contract Manufacturing, Data Analysis, Dental Insurance, Documentation, External Audit, Failure Mode and Effects Analysis (FMEA), GMP (Good Manufacturing Practices), Health Insurance, Healthcare, ISO (International Organization for Standardization), Internal Audit, Lean Manufacturing, Life Insurance, Manufacturing, Manufacturing/Industrial Processes, Materials Testing, Medical Equipment, Operations Processes, Product Testing, Product/Service Launch, Quality Engineering, Quality Management, Risk Management, Software Testing, Systems Maintenance, Technical Support, Testing, Vision Plan
Join Our Team at Trelleborg Medical Solutions!
Imagine working for one of the leading contract manufacturers in the world, nestled just 30 miles from California’s stunning Central Coast. At Trelleborg Medical Solutions, we are not just a premier manufacturer of life-saving medical components; we are a forward-thinking company committed to excellence and innovation. Our journey in lean manufacturing has been ongoing for years, and we are on the path to becoming a showcase of excellence in the medical industry.
Seize this rare opportunity to be part of a medical solutions business with over 100 years of history, all
while enjoying the benefits of living in one of California’s most desired locations!
Why join us?
As a valued Trelleborg team member, you will enjoy:
- Life Insurance
- Medical Insurance
- Vision Insurance
- Dental Insurance
- 401(k) plan
- Generous PTO plan
- 12 paid holidays
Position: Quality Engineering Technician
Trelleborg Medical Solutions is currently accepting applications for a Quality Assurance Technician. This role will partner with Quality Engineers in developing, trouble shooting, standardizing and improving new and existing production methods and procedures for new product release and legacy products. Follow good manufacturing practices (GMP) and principles to help develop and maintain the quality system.
Key Responsibilities:
- Assists Engineers with the tasks related to the development and/or update of Risk Management FMEA and similar documentation
- Supports Engineering group in development and performance of equipment installation, software, and operational qualifications and process operational and process qualifications for customer manufacturing processes
- Performs data analysis, researching, compiling and analyzing information and assists in GR&R activities. Creates measurement system programs, when necessary
- Communicates quality issues to Quality Engineers
- Supports internal and external audit activities
- Performs product and material testing, as needed.
- Other duties as assigned
Education and Experience
Required:
- 2 year degree in quality, manufacturing, engineering, or related equivalent experience
- Regulated manufacturing industry experience
Desired:
- 2+ years of regulated manufacturing experience.
- Quality certification(s) (e.g. ASQ CQE, CQT, CQA, etc.).
- Class I, II and/or III Medical Device manufacturing experience.
- Knowledge and experience with GMP/ISO Standards.
Salary: $60,000 - $70,000
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