ZipRecruiter

Log In

1

Process Validation Manager Pharmaceutical Jobs (NOW HIRING)

Unifin SAS

Validation Specialist

Rochester, NY · On-site

As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve ... processes, equipment, utilities, and facilities in a regulated environment. This role manages ...

RXinsider LTD.

Sr. Manager, Validation

Bedford, OH · On-site

$92K - $158K/yr

Sr. Validation Manager Bedford, Ohio Full-time About Us As a developer, manufacturer, and supplier ... in the pharmaceutical or other GMP-regulated industry * Experience with aseptic processes is ...

INCOG

Senior Process Validation Engineer

Fishers, IN · On-site

$97K - $125K/yr

... teams and manage customer communications. Recognized as Subject Matter Expert for multiple ... matters of process validation and mentor Entry Level engineers - Conduct comprehensive impact ...

Danaher

Process Validation Engineering Co-Op

Fargo, ND · On-site

$30/hr

This position reports to the Manager, Process Validation and is part of the Technical Operations team located in Fargo, North Dakota and will be an on-site role. In this role, you will have the ...

Scorpion Therapeutics

NY · On-site

Collaborates with Manufacturing, QC, QA, and CMC Regulatory to support process lifecycle management ... Ensures SOPs, policies, and validation plans align with industry and regulatory standards (e.g ...

previous page

Showing results 41-60

All JobsManufacturing JobsProduct Manufacturing JobsValidation Engineer JobsProcess Validation Manager Pharmaceutical Jobs

Process Validation Manager Pharmaceutical information

See salary details

$47.5K

$105.4K

$160.5K

How much do process validation manager pharmaceutical jobs pay per year?

As of Sep 12, 2026, the average yearly pay for process validation manager pharmaceutical in the United States is $105,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $132,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Process Validation Manager Pharmaceutical jobs?

For Process Validation Manager Pharmaceutical jobs, the most frequently searched job titles are:

Infographic showing various Process Validation Manager Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.

Engineer III, Validation - Process & Cleaning

Greenville, NC • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees
Learn more about Thermo Fisher Scientificexternal

Full-time

Re-posted 7 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 431 frontline employees who took The Breakroom Quiz

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
Job Description
Discover Impactful Work:
Join Thermo Fisher Scientific and be part of a team delivering life-changing therapies through world-class sterile pharmaceutical manufacturing.
As a Validation Engineer III, you will lead validation activities supporting process and cleaning validation in sterile environments, playing a key role in ensuring compliance, quality, and successful product launches.
This role offers high visibility and cross-functional exposure, working across Operations, Quality, and QC Labs-often acting as a technical lead during tech transfers and validation execution.
A Day in the Life:
  • ~70% desk-based: protocol writing, data analysis, deviation investigations, reporting
  • ~30% on the floor: executing validation in sterile manufacturing environments
  • Lead validation activities including:
    • Process validation
    • Cleaning validation
    • Equipment qualification (IQ/OQ/PQ)
  • Support tech transfers and new product introductions
  • Collaborate cross-functionally with Ops, QC, and Quality teams
  • Participate in client interactions, audits, and regulatory readiness

What to Expect:
  • Ownership of complex validation projects
  • High exposure across site operations and leadership teams
  • Opportunity to act in a project management capacity
  • Involvement in audits, deviations, and continuous improvement

Keys to Success:
Education & Experience:
  • Bachelor's degree and 4+ years validation experience
  • Experience in pharmaceutical or biotech manufacturing required
  • Direct experience in sterile/aseptic pharmaceutical manufacturing highly preferred:
    • Aseptic filling
    • Sterile processing
    • Cleanroom environments

Skills & Expertise:
  • Strong experience with:
    • Process validation
    • Cleaning validation
    • Equipment qualification (IQ/OQ/PQ)
  • Proven ability to write and execute validation protocols and reports
  • Experience with validation documentation and regulatory standards
  • Exposure to audits, audit responses, or regulatory inspections
  • Strong problem-solving and deviation investigation skills
Preferred:
  • Experience in both process and cleaning validation
  • Background in sterile filling or manufacturing operations
  • Knowledge of FDA, EMA, and cGMP regulations
Work Environment & Requirements:
  • Onsite role in Greenville, NC
  • Monday-Friday schedule with flexibility as needed
  • Cleanroom and production floor exposure required
Why Join Us:
  • Work on cutting-edge sterile pharmaceutical programs
  • Gain broad cross-functional exposure across the site
  • Be part of high-impact tech transfers and product launches
  • Clear path to senior and leadership roles

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply