Quality Assurance Supervisor: Compliance & Process Leader

LifeScience Logistics LLC.; Indiana (PA); On-site; USD 70,000 - 110,000; Full time

Job summary

LifeScience Logistics LLC. seeks a Quality Leader to manage change requests, CAPAs, deviations, and the internal audit program in a regulated environment.

This role supervises staff, mentors team members, and ensures compliance with FDA/ISO requirements while supporting a temperature-controlled warehouse. Qualified candidates have a BS in engineering/science, 3–5 years in quality roles within medical devices or pharma, plus 2+ years supervisory experience and strong communication and analytical

Qualifications

• B.S. degree in Engineering, Science or related field preferred.
• 3–5 years of quality experience in medical device/pharma or regulated industry.
• At least 2 years of supervisory experience.
• Demonstrated research ability, strong communication, and analytical skills.
• Detail orientation, organization, and critical thinking.

Responsibilities

• Lead quality processes: changes, CAPAs, deviations.
• Mentor and coach direct reports to support career goals.
• Support audit programs and regulatory compliance.
• Assist with DEA program and client audits.
• Provide QA metrics and identify adverse trends.
• Train on quality documents and procedures.
• Collaborate with cross-functional teams in a warehouse/office setting.

Skills

Verbal communication

Written communication

Analytical skills

Attention to detail

Critical thinking

Ability to work in fast-paced env

Research ability

Education

B.S. in Engineering/Science or related field

Tools

CQ (Quality Management Software)

Tecsys Elite

WebCTRL

Job description

LifeScience Logistics LLC. seeks a Quality Leader to manage change requests, CAPAs, deviations, and the internal audit program in a regulated environment.

This role supervises staff, mentors team members, and ensures compliance with FDA/ISO requirements while supporting a temperature-controlled warehouse. Qualified candidates have a BS in engineering/science, 3–5 years in quality roles within medical devices or pharma, plus 2+ years supervisory experience and strong communication and analytical