Staff Validation Engineer Greenville NC

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

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Health Flexible Spending Account

Dependent Care Flexible Spending Array

Supplemental Life Insurance

Short Term and Long Term Disability

Business Travel Insurance

401(k), Plus Match

Weekly Pay

Job summary

Our client in the pharmaceutical/biotech sector is seeking a Staff Validation Engineer to join the Validation and Quality organization in Greenville, NC. You will lead aseptic validation initiatives and contribute to contamination control programs, ensuring compliance with cGMP and global regulatory expectations.

The role emphasizes technical leadership, cross-functional collaboration, and clear communication to advance sterile manufacturing readiness and patient safety in a fast-paced

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related field.
• 8+ years of pharmaceutical/biotech validation experience.
• Strong aseptic processing and media fill execution experience; sterile manufacturing familiarity; strong technical writing.

Responsibilities

• Lead the design and execution of media fill (APS) studies for aseptic manufacturing processes.
• Author and review validation protocols, reports, and risk assessments.
• Support investigations, deviations, and CAPAs related to media fills and aseptic processes.
• Partner cross-functionally with Manufacturing, Quality, and Regulatory teams.
• Drive continuous improvement in validation and contamination control while ensuring compliance with cGMP and regulatory expectations.

Skills

Aseptic processing

Media fill execution

Technical writing

Cross-functional leadership

cGMP compliance

Education

Bachelor's degree in Engineering, Life Sciences, or related field

Job description

Our client, pharmaceutical and biotech manufacturing is seeking a Staff Validation Engineer to join their team. As a Staff Validation Engineer, you will be part of the Validation and Quality organization supporting aseptic processing validation and contamination control initiatives. The ideal candidate will have strong technical leadership, a commitment to cGMP compliance, and the ability to communicate clearly across cross‑functional teams, which will align successfully in the organization. Job Title: Staff Validation Engineer. Location: Greenville, NC. Pay Range: $50/hr.

What's the Job?

• Lead the design and execution of media fill (APS) studies for aseptic manufacturing processes.
• Author and review validation protocols, reports, and risk assessments to support sterile manufacturing readiness.
• Support investigations, deviations, and CAPAs related to media fills and aseptic processes.
• Partner cross‑functionally with Manufacturing, Quality, and Regulatory teams to ensure alignment and timely execution.
• Drive continuous improvement initiatives in validation and contamination control strategies while maintaining compliance with cGMP and global regulatory expectations.

What's Needed?

• Bachelor's degree in Engineering, Life Sciences, or a related field.
• 8+ years of experience in pharmaceutical/biotech validation.
• Strong experience with aseptic processing and media fill execution (required).
• Experience in sterile manufacturing environments (required).
• Deep understanding of aseptic processing and contamination control, including strong technical writing skills for validation protocols and reports.

What's in it for me?

Opportunity to lead complex media fill (APS) validation work that directly supports patient safety and product quality. Chance to strengthen your impact by partnering with Manufacturing, Quality, and Regulatory teams on investigations and CAPAs. Work in a compliance‑focused environment aligned with cGMP and FDA/EMA expectations. Use your independent project leadership skills to drive continuous improvement in contamination control and validation strategies. Build credibility through clear, accurate documentation and risk‑based decision‑making across validation deliverables.

Benefits

Upon completion waiting period consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay