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Biotech Validation Jobs (NOW HIRING)

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

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

Senior Validation Engineer

Durham, NC · On-site

$120K - $140K/yr

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 ...

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As of Sep 11, 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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Infographic showing various Biotech Validation job openings in the United States as of September 2026, with employment types broken down into 93% Full Time, 3% Part Time, 1% Temporary, and 3% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Staff Validation Engineer, Media Fills

Greenville, NC

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

Full-time

Re-posted 15 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 430 frontline employees who took The Breakroom Quiz

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

Pay

Benefits

Hours and flexibility

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