Sr. Quality Engineer

B. Braun Group

Carrollton (TX)

On-site

USD 105,000 - 115,000

Full time

2 days ago
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Benefits offered by this job

Health insurance
401(k) plan
Tuition reimbursement

Job summary

B. Braun US Device Manufacturing LLC in Carrollton, TX, is seeking a Senior Quality Engineer with medical device industry experience to strengthen our Quality Management System and drive continuous improvement across cross-functional teams.

You will lead CAPA investigations, audits, and change control, ensure FDA and ISO 13485 compliance, and partner with Engineering and Manufacturing to deliver safe, high-quality medical products.

Qualifications

  • Bachelor's degree in Engineering, Quality, Life Sciences, or related field.
  • 6+ years of Quality Engineering experience in a regulated manufacturing environment.
  • Medical Device industry experience required.
  • Professional quality certification (ASQ CQE, CQA, or equivalent).

Responsibilities

  • Lead and support quality system activities, including: Nonconformances, CAPA investigations, Complaint investigations and trend analysis, Change control, Validation activities, Quality inspections, MRB activities, Internal audits.
  • Conduct root cause investigations and implement effective corrective actions.
  • Collaborate with Engineering, Manufacturing, and other teams to identify and mitigate quality risks.
  • Ensure compliance with FDA regulations, ISO 13485, and internal quality standards.
  • Audit processes, suppliers, and materials to ensure quality requirements are met.
  • Drive continuous improvement and quality enhancement projects.
  • Analyze quality data and recommend process improvements.

Skills

QMS knowledge
CAPA investigations
Root Cause Analysis
Change Control
Validation
Internal Auditing
Complaint Handling

Education

Bachelor's degree in Engineering, Quality, Life Sciences, or related field

Tools

SAP

Job description

You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.

Sr. Quality Engineer

Company: B. Braun US Device Manufacturing LLC

Functional Area: Quality

Working Model: Onsite

Days of Work: Wednesday, Tuesday, Friday, Thursday, Monday

Shift: 5X8

Relocation Available: No

Requisition ID: 13418

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®.

Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit www.bbraunusa.com

Senior Quality Engineer

Make a Difference in Quality and Patient Safety

We are seeking a Senior Quality Engineer with medical device industry experience to support and continuously improve our Quality Management System (QMS). In this role, you will partner with cross-functional teams to ensure compliance, drive quality excellence, and lead process improvement initiatives that support safe and effective products.

Key Responsibilities
  • Lead and support quality system activities, including:
    • Nonconformances
    • CAPA investigations
    • Complaint investigations and trend analysis
    • Change control
    • Validation activities
    • Quality inspections
    • Material Review Board (MRB) activities
    • Internal audits
  • Conduct root cause investigations and implement effective corrective actions.
  • Collaborate with Engineering, Manufacturing, and other teams to identify and mitigate quality risks.
  • Ensure compliance with FDA regulations, ISO 13485, and internal quality standards.
  • Audit processes, suppliers, and materials to ensure quality requirements are met.
  • Drive continuous improvement and quality enhancement projects.
  • Analyze quality data and recommend process improvements.

Required Qualifications
  • Bachelor's degree in Engineering, Quality, Life Sciences, or a related field.
  • 6+ years of Quality Engineering experience in a regulated manufacturing environment.
  • Medical Device industry experience required.
  • Professional quality certification (ASQ CQE, CQA, or equivalent).
  • Strong knowledge of:
    • Quality Management Systems (QMS)
    • CAPA
    • Root Cause Analysis
    • Change Control
    • Validation
    • Internal Auditing
    • Complaint Handling

Preferred Qualifications
  • Experience with SAP.
  • Experience leading projects, teams, or continuous improvement initiatives.
  • Knowledge of Lean Manufacturing or Six Sigma methodologies.
  • Experience supporting regulatory audits and inspections.
    Additional Information
    • Ability to work non-standard hours as needed to support business objectives.
    • Commitment to maintaining a safe work environment and following all company safety policies.
    • Must be able to perform the essential functions of the position with or without reasonable accommodation.

    Salary Range: $105,300 - $115,300

The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.

B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com .

Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.

We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here .

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