Now Hiring: Quality Assurance Specialist (2nd Shift)

Location: Mebane, NC 27302

Company: Becton Dickinson (BD)

Job Type: Contract

Shift: 2nd Shift | Monday – Friday | 3:00 PM – 11:30 PM (Onsite)

Duration: July 6, 2026 – October 30, 2026 (Potential for extension based on business needs)

Pay Rate: $27.10 – $27.50 per hour

Schedule: 40 hours per week

About the Opportunity

Becton Dickinson (BD), a global leader in medical technology and life sciences, is seeking a Quality Assurance Specialist to join its Liquid Media Manufacturing team in Mebane, NC.

This is an excellent opportunity for quality professionals with experience in FDA-regulated or ISO 13485 manufacturing environments who enjoy working directly on the production floor to ensure product quality, regulatory compliance, and continuous process improvement.

The Quality Assurance Specialist serves as the on-floor quality representative, partnering closely with Manufacturing, Quality Control, Engineering, and Maintenance teams to support daily production while maintaining compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).

Job Responsibilities

As a Quality Assurance Specialist, you will:

• Provide daily quality support on the manufacturing floor.

• Verify line setup and perform line clearance activities.

• Conduct in-process quality inspections and spot checks.

• Review production documentation in real time for accuracy, completeness, and compliance.

• Ensure adherence to Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).

• Identify documentation errors and process deviations.

• Detect, document, and help contain nonconforming conditions.

• Escalate quality risks and compliance concerns to appropriate teams.

• Assist with investigations by gathering facts and reviewing documentation.

• Coordinate sample preparation and submission to the Quality Control laboratory.

• Work collaboratively with Manufacturing, Engineering, Maintenance, and QC teams to resolve quality issues.

• Provide guidance to production associates regarding quality standards and documentation requirements.

• Promote defect prevention and continuous quality improvement initiatives.

Required Qualifications

• Bachelor's degree OR an Associate degree with additional manufacturing/quality experience.

• Minimum 2 years of experience in Manufacturing or Quality within an FDA-regulated or ISO 13485 environment.

• Experience performing inspections, production support, or documentation review.

• Working knowledge of:

  • Good Manufacturing Practices (GMP)

  • Good Documentation Practices (GDP)

• Strong attention to detail with the ability to identify documentation errors and nonconformances.

• Ability to work independently in a fast-paced manufacturing environment.

• Strong written and verbal communication skills.

• Basic computer proficiency, including Microsoft Office.

Preferred Qualifications

• Experience supporting production floor quality activities.

• Knowledge of sampling plans and inspection standards.

• Familiarity with nonconformance processes.

• Experience working in medical device, pharmaceutical, biotechnology, diagnostics, or other regulated manufacturing industries.

Required Skills

• Quality Assurance

• GMP (Good Manufacturing Practices)

• GDP (Good Documentation Practices)

• FDA-Regulated Manufacturing

• ISO 13485

• Documentation Review

• In-Process Inspection

• Production Floor Support

• Quality Inspection

• Line Clearance Verification

• Compliance Monitoring

• Nonconformance Identification

• Quality Documentation

• Investigation Support

• Microsoft Office

• Cross-Functional Collaboration

• Problem Identification

• Critical Thinking

• Attention to Detail

• Communication Skills

Work Environment

• Primarily on the manufacturing production floor.

• Standing and walking for extended periods.

• Working in a controlled manufacturing environment.

• Use of required Personal Protective Equipment (PPE).

• Fast-paced, team-oriented environment.

Schedule

• Monday – Friday

• 2nd Shift

• 3:00 PM – 11:30 PM

• 40 hours per week

• 100% Onsite (No remote or hybrid option)

Interview Process

• In-person interviews are preferred.

• Phone or video interviews may be considered.

Why Join BD?

• Competitive hourly pay.

• Opportunity to work with a global leader in medical technology.

• Gain valuable experience in a highly regulated manufacturing environment.

• Collaborative team culture with opportunities to expand your quality and compliance expertise.

If you have experience in Quality Assurance, GMP/GDP compliance, FDA-regulated manufacturing, or ISO 13485 environments and are looking for your next opportunity, we'd love to hear from you!