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Biotech Validation Jobs (NOW HIRING)

Valspec

Validation Engineer

Los Angeles, CA

$90K - $110K/yr

Validation Engineer (CQV) El Segundo, CA | Onsite | 6-Month Project | Start Date: November 2, 2026 ... Located in the heart of Southern California's biotech and aerospace corridor, El Segundo offers ...

Valspec

Validation Engineer

Palos Verdes Estates, CA · On-site

$90K - $110K/yr

Validation Engineer (CQV) El Segundo, CA | Onsite | 6-Month Project | Start Date: November 2, 2026 ... Located in the heart of Southern California's biotech and aerospace corridor, El Segundo offers ...

Valspec

Validation Engineer

Long Beach, CA

$90K - $110K/yr

Validation Engineer (CQV) El Segundo, CA | Onsite | 6-Month Project | Start Date: November 2, 2026 ... Located in the heart of Southern California's biotech and aerospace corridor, El Segundo offers ...

Stark Pharma Solutions Inc

MD · On-site

Hands-on experience in GMP pharmaceutical or biotechnology manufacturing . * Strong knowledge of IQ/OQ/PQ , cGMP, GDP, and validation lifecycle. * Experience with aseptic processing , cleanrooms ...

Pinnaql

Validation Engineer

Barceloneta, PR · On-site

We are seeking a Validation Engineer with hands-on experience in biotech/pharmaceutical manufacturing, specifically supporting aseptic filling operations (vials). This role will be responsible for ...

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How much do biotech validation jobs pay per hour?

As of Sep 12, 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.

Validation Engineer

Cincinnati, OH

Validation & Engineering Group, Inc
See more jobs at Validation & Engineering Group, Incexternal

Full-time

Re-posted 22 hours ago

Key responsibilities

  • Lead full validation lifecycle activities including FAT, SAT, CSV, equipment integration, and startup.

  • Develop User Requirement Specifications (URS) and create engineering documentation.

  • Manage equipment commissioning, qualification, and ensure compliance with safety, regulatory, and GMP standards.

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer

Description:

The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.

Key Responsibilities:

  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:

  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.