Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

Process Validation Engineer

Job

ELIQUENT Life Sciences

Greenville, NC (In Person)

Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 7/24/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
73
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Process Validation Engineer at
ELIQUENT
Life Sciences Process Validation Engineer at
ELIQUENT
Life Sciences in Greenville, North Carolina Posted in 1 day ago.
Type:
full-time
Job Description:
ELIQUENT
Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world.
ELIQUENT
is committed to serving clients' needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com. We are seeking a Process Validation Engineer to support pharmaceutical manufacturing projects, including a new fill line implementation and revalidation activities.
Key Responsibilities:
  • Develop and execute process validation strategies for new fill line projects
  • Support Process Performance Qualification (PPQ) studies and validation activities
  • Coordinate and evaluate aseptic media fill runs
  • Perform revalidation activities for pre-filled syringe (PFS) fill lines
  • Support tech transfer projects across new and existing manufacturing lines
  • Conduct risk assessments and ensure cGMP compliance
  • Support CQV, qualification, and validation documentation activities
  • Conduct and support smoke studies for aseptic processing environments
  • Support qualification of automated visual inspection systems
Required Skills:
  • Process Validation
  • Validation Protocol Development & Execution
  • Smoke Studies
  • Pharmaceutical Manufacturing Experience
  • cGMP Knowledge
Strong Documentation & Communication Skills Preferred Skills:
  • PPQ Experience
  • Pre-Filled Syringe (PFS) Fill Line Experience
  • Media Fill Support
  • CQV / Qualification Experience
  • Tech Transfer Experience
  • Automated Visual Inspection Qualification