QA Engineer, Senior I

$86,000 - $108,000/Yr

B. Braun Group - Carrollton, TX

posted 3 months ago

Full-time - Mid Level
Carrollton, TX
251-500 employees
Warehousing and Storage

About the position

B. Braun Medical Inc., a leader in infusion therapy and pain management, is seeking a Senior QA Engineer to join our team in Carrollton, TX. This position plays a critical role in ensuring the quality and safety of our medical products and services. The Senior QA Engineer will establish quality standards for products and processes, working closely with cross-functional teams including product design, product management, and production to identify and mitigate quality risks. The role involves auditing production processes, raw materials, and suppliers to ensure compliance with established quality standards, and conducting root cause analysis for defects and non-conformities. The successful candidate will also be responsible for ensuring compliance with formal external quality standards, such as ISO 9001, and will be expected to take reasonable care for the safety and health of themselves and others while at work. In this role, the Senior QA Engineer will utilize advanced knowledge of the professional field and industry to influence the development and application of quality principles and concepts. The position requires minimal supervision, relying on experience and judgment to plan and accomplish assigned goals. The Senior QA Engineer will also assist in orienting, training, and reviewing the work of peers, and will have frequent contact with external contractors and vendors. The targeted salary range for this position is between $86,000 and $108,000, depending on experience and qualifications. B. Braun Medical Inc. is committed to eliminating preventable treatment errors and enhancing patient, clinician, and environmental safety. We are looking for a dedicated professional who shares our commitment to quality and safety in healthcare.

Responsibilities

  • Establish quality standards for products and processes and suggest modifications to prevent defects.
  • Work closely with cross-functional teams to identify and mitigate quality risks.
  • Audit production processes, raw materials, and suppliers to ensure compliance with quality standards.
  • Conduct root cause analysis for defects and non-conformities.
  • Ensure compliance with formal external quality standards, such as ISO 9001.
  • Perform other responsibilities as assigned by the Supervisor.

Requirements

  • Bachelor's degree required.
  • 08-10 years related experience required.
  • Applicable industry/professional certification preferred.
  • Regular and predictable attendance is required.
  • Occasional business travel may be required.

Nice-to-haves

  • Experience in the medical device industry.
  • Knowledge of FDA regulations and quality system requirements.

Benefits

  • Healthcare coverage
  • 401(k) plan
  • Tuition reimbursement
  • Paid time off
  • Employee discounts
  • Flexible scheduling options
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service