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Validation Engineer Biologics Jobs (NOW HIRING)

Pinnaql

Validation Engineer

Barceloneta, PR · On-site

Bachelor's degree in Engineering, Chemistry, Biology, or related field. * 3 7+ years of validation experience in biotech or pharmaceutical industry. * Strong experience with: * Aseptic processing

Forge Biologics

Validation Engineer I

Columbus, OH · On-site

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is ... As a Validation Engineer I , you will be responsible for the design, implementation, and execution ...

Forge Biologics

Validation Engineer I

Columbus, OH · On-site

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is ... As a Validation Engineer I , you will be responsible for the design, implementation, and execution ...

Forge Biologics

Validation Engineer I

Columbus, OH

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is ... As a Validation Engineer I , you will be responsible for the design, implementation, and execution ...

ADMA Biologics

Engineer, Validation

Boca Raton, FL · On-site

ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products ... Engineer, Validation Position Summary The Engineer, Validation provides validation support to ...

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The Validation Engineer ...

Quality Agents

Validation Engineer II

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The Validation Engineer ...

Generis TEK Inc.

Validation Engineer

Carlsbad, CA · On-site

$48/hr

Qualification and validation of GMP manufacturing equipment used in oligonucleotide, biologics, or ... engineering studies, process validation protocols, validation reports, and final validation ...

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...

Evotec WD

Validation Engineer III

Redmond, WA · On-site

$115K - $126K/yr

... biologics manufacturing within a fast‑paced, global validation team. You will also support the ... Bachelor's degree in engineering science or a related program. * 7+ years of relevant experience as ...

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How much do validation engineer biologics jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for validation engineer biologics 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.

What are popular job titles related to Validation Engineer Biologics jobs?

For Validation Engineer Biologics jobs, the most frequently searched job titles are:

Infographic showing various Validation Engineer Biologics job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Barceloneta, PR • On-site

Validation & Engineering Group, Inc.
See more jobs at Validation & Engineering Group, Inc.external

Full-time

Re-posted 18 days ago

Key responsibilities

  • Develop, review, and execute validation protocols for aseptic filling lines, lyophilization, and support equipment.

  • Perform process validation activities related to sterile manufacturing, including media fills, and support commissioning and qualification activities for new equipment and facility upgrades.

  • Investigate deviations, CAPAs, and implement corrective actions related to validation activities.

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company 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:
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 executing and supporting validation activities for equipment, processes, and computerized systems in compliance with regulatory requirements and industry standards.
Responsibilities:
  • Develop, review, and execute validation protocols including IQ, OQ, PQ for:
    • Aseptic filling lines (vial filling, stoppering, capping)
    • Lyophilization (if applicable)
    • Support equipment (autoclaves, washers, depyrogenation tunnels)
  • Perform process validation activities related to sterile manufacturing, including media fills (APS).
  • Ensure compliance with cGMP, FDA, EMA, and ICH guidelines.
  • Support commissioning and qualification (C&Q) activities for new equipment and facility upgrades.
  • Generate and review:
    • Validation master plans (VMPs)
    • SOPs, protocols, and final reports
  • Collaborate with cross-functional teams (Manufacturing, QA, Engineering, MSAT).
  • Investigate deviations, CAPAs, and implement corrective actions related to validation activities.
  • Support risk assessments (FMEA, impact assessments) for validation scope.
  • Ensure data integrity and adherence to 21 CFR Part 11 requirements (if applicable to systems).

Qualifications:
  • Bachelor's degree in Engineering, Chemistry, Biology, or related field.
  • 3�7+ years of validation experience in biotech or pharmaceutical industry.
  • Strong experience with:
    • Aseptic processing
    • Vial filling operations
    • Sterile manufacturing environments
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • Available to work extended hours, possibility of weekends and holidays.

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.

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