Lead Aseptic Validation Engineer for Media Fill

Experis (Austria); Greenville (NC); On-site; USD 57,000 - 81,000; Full time

Job summary

ManpowerGroup is seeking a Staff Validation Engineer for a pharmaceutical/biotech client in Greenville, NC. You will lead aseptic validation, oversee media fills, and author validation protocols to support sterile manufacturing readiness.

Strong technical leadership, cGMP knowledge, and clear cross‑functional communication are essential to drive investigations, CAPAs, and continuous improvement aligned with FDA/EMA expectations.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• 8+ years in pharmaceutical/biotech validation.
• Strong aseptic processing and media fill experience.

Responsibilities

• Lead design and execution of media fill studies for aseptic manufacturing.
• Author and review validation protocols, reports, and risk assessments.
• Support investigations, deviations, and CAPAs related to aseptic processes.
• Collaborate with Manufacturing, Quality, and Regulatory teams for timely execution.
• Drive continuous improvement while maintaining cGMP and regulatory compliance.

Skills

Aseptic processing

Media fill execution

Validation

Technical leadership

cGMP compliance

Education

Bachelor's degree in Engineering or Life Sciences

Job description

ManpowerGroup is seeking a Staff Validation Engineer for a pharmaceutical/biotech client in Greenville, NC. You will lead aseptic validation, oversee media fills, and author validation protocols to support sterile manufacturing readiness.

Strong technical leadership, cGMP knowledge, and clear cross‑functional communication are essential to drive investigations, CAPAs, and continuous improvement aligned with FDA/EMA expectations.