Drimva

Novartis

Validation Lead

$126K–$234K

Morrisville (North Carolina) · Full-time · Posted Sep 28, 2026

Experience
8 years in the stated pharmaceutical fields and setting; 5 years executing process validation, including leading and managing projects.
Education
Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or a related scientific discipline.

About the job

Leads the Morrisville site’s pharmaceutical validation strategy and programs to ensure manufacturing quality, compliance, and readiness for launches, transfers, and inspections.

What you'll do

  • Lead validation across process, cleaning, packaging, and ongoing verification; own the Validation Master Plan and performance metrics.
  • Provide technical leadership for risk assessments, investigations, and complex validation challenges, and define interfaces with related qualification and validation work.
  • Support product launches and technical transfers, and represent the site in audits, inspections, and validation governance.

What they ask for

  • Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or a related scientific discipline.
  • 8 years of experience in manufacturing, manufacturing science and technology, technical development, or quality in oral solid dosage pharmaceutical manufacturing.
  • 5 years of experience executing process validation, including leading and managing validation projects.
  • Expertise in process validation, cleaning validation, and ongoing process verification; knowledge of quality systems, applied statistics, and global regulatory requirements.

Nice to have

  • PhD in Chemistry, Pharmacy, Chemical Engineering, or Pharmaceutical Technology; or equivalent.

Pay

$126,000 and $234,000 per year (base salary); $126,000.00 - $234,000.00 (base salary)

Tools

Validation Master Plan, applied statistics

Model-written summary · the original posting is authoritative

First seen Oct 28, 2026 · Last verified Nov 5, 2026 (UTC)