Quality Assurance Lead: Device Assembly & Packaging

BioSpace; Concord (NC); On-site; USD 65,000 - 169,000; Full time

Benefits offered by this job

401(k)

Pension

Vacation benefits

Medical, dental, vision

Flexible benefits

Life insurance

Time off and leave

Job summary

Lilly is seeking a Quality Assurance Process team member to lead quality oversight in manufacturing areas such as Device Assembly, Packaging, and Project Focus for DAP. You will mentor operations staff, review deviations, change controls, and ensure testing and qualification activities meet quality standards.

Join a global team committed to patient well-being; candidates should have a Bachelor's in a scientific field, 4+ years in pharmaceutical QA, and experience with GxP, C&Q, and computer

Qualifications

• Bachelor's degree in a scientific field is required.
• 4+ years of experience in quality pharmaceutical manufacturing.
• Experience with C&Q, verification and validation, including automation and computer systems validation.
• Must be legally authorized to work in the United States.

Responsibilities

• Lead, mentor, and coach operations on quality matters.
• Provide support on deviations, change controls, and procedure updates.
• Oversee verification and qualification of equipment, buildings, and computer systems.
• Monitor and ensure compliance to quality standards in operations.
• Develop and manage the annual quality floor time plan.
• Identify and implement continuous improvements.

Skills

Quality assurance

GxP compliance

Process validation

Deviation management

Education

Bachelor's degree in a scientific field

Tools

SAP

TrackWise

MES

Job description

Lilly is seeking a Quality Assurance Process team member to lead quality oversight in manufacturing areas such as Device Assembly, Packaging, and Project Focus for DAP. You will mentor operations staff, review deviations, change controls, and ensure testing and qualification activities meet quality standards.

Join a global team committed to patient well-being; candidates should have a Bachelor's in a scientific field, 4+ years in pharmaceutical QA, and experience with GxP, C&Q, and computer