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Biotech Validation Jobs (NOW HIRING)

PSC Biotech

Validation Engineer

Minneapolis, MN · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... The Validation Engineer will collaborate with cross-functional teams to support project execution ...

PSC Biotech

Validation Engineer

Minneapolis, MN · On-site

$90 - $105/hr

At PSC Biotech, it's about more than just a job--it's about your career and your future. Your Role We are seeking a Validation Engineer to support the validation of facilities, utilities, and ...

PSC Biotech

Senior Validation Engineer

Durham, NC · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... This individual will lead validation lifecycle activities, including protocol development ...

PSC Biotech

Validation QA Specialist

Pomona, CA

$110K - $120K/yr

At PSC Biotech, it's about more than just a job-it's about your career and your future. Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation ...

PSC Biotech

Validation Engineer

Minneapolis, MN · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... The Validation Engineer will collaborate with cross-functional teams to support project execution ...

PSC Biotech

Validation Engineer

Minneapolis, MN

$90K - $105K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... The Validation Engineer will collaborate with cross-functional teams to support project execution ...

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How much do biotech validation jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for biotech validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
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Biotech Validation jobs near you
Infographic showing various Biotech Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 4% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Staff Validation Engineer, Media Fills

Thermo Fisher Scientific

Greenville, NC • On-site

Full-time

Re-posted 24 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

200th of 540 rated manufacturers

Job description

Work Schedule
First Shift (Days)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact?
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. The Staff Engineer, Media Fill plays a critical role in supporting sterile/aseptic manufacturing operations by leading media fill (aseptic process simulation) programs. This role ensures processes remain in a validated state and compliant with global regulatory expectations.
What will you do?
  • 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
  • Ensure compliance with cGMP, FDA, EMA, and global regulatory requirements
  • Drive continuous improvement initiatives in validation and contamination control strategies

How will you get here?
Education:
  • Bachelor's degree in Engineering, Life Sciences, or related field

Experience:
  • 8+ years of experience in pharmaceutical/biotech validation
  • Strong experience with aseptic processing and media fill execution (required)
  • Experience in sterile manufacturing environments (required)

Knowledge, Skills, Abilities:
  • Deep understanding of aseptic processing and contamination control
  • Strong knowledge of cGMP and regulatory expectations
  • Technical writing expertise (validation protocols and reports)
  • Ability to lead complex validation projects independently
  • Strong collaboration and communication skills

What Thermo Fisher Scientific employees say

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Hours and flexibility

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