QC Inspector II Night Shift; Green Team) Injection Molding

QC Inspector II - 12

Hr. Night Shift (Green Team) Injection Molding 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.

QC Inspector II - 12

Hr. Night Shift (Green Team) Injection Molding Company:

B. Braun US Device Manufacturing LLC Job Posting

Location:

Allentown, Pennsylvania, United States

Functional Area:

Quality Working Model:
Onsite Days of Work:
Rotating Shift: 3/4 X 12 Relocation Available:
No Requisition

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

Job Summary:
B. Braun is seeking a detail-oriented
Quality Inspector II to support our quality operations in a fast-paced manufacturing environment. In this role, you will perform inspections, audits, testing, and documentation activities that help ensure products meet regulatory, customer, and company quality standards.

This is an excellent opportunity for quality professionals who enjoy hands-on work, problem-solving, and contributing to a culture of continuous improvement.

Key Responsibilities:

• Perform inspections, testing, and sampling of raw materials, components, subassemblies, and finished products.
• Verify products meet established quality specifications and acceptance criteria.
• Document inspection and testing results accurately and maintain quality records.
• Review batch records and ensure compliance with quality requirements.
• Identify, segregate, and support disposition of non-conforming materials.
• Conduct quality audits to ensure adherence to procedures and standards.
• Coordinate calibration activities for inspection and testing equipment.
  
  Assist with creating and updating inspection procedures, protocols, and checklists.
• Partner with cross-functional teams to maintain product quality and compliance.
• Support continuous improvement initiatives within the Quality organization.

• High School Diploma or GED required.
• 2+ years of experience in Quality, Manufacturing, Inspection, or a related field.
• Strong attention to detail and commitment to quality.
• Ability to read, interpret, and follow procedures and work instructions.
• Basic computer and documentation skills.
• Ability to work effectively in both manufacturing and office environments.

• Associate degree or technical degree.
• Experience in a regulated manufacturing environment (medical device, pharmaceutical, or similar industry).
• Industry or quality-related certifications.
• Experience reviewing production documentation or batch records.