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Validation Consultant Jobs (NOW HIRING)

Valspec

CQV Consultant

Collegeville, PA

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

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Valspec

CQV Consultant

Charlotte, NC · On-site

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

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Intellectt INC

CQV Consultant

Los Angeles, CA · On-site

CQV Consultant Location: Los Angeles, CA Job Summary: We're looking for a Facilities CQV ... Cleaning Validation is highly preferred (to provide backup support as needed). Day-to-day ...

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Valspec

CQV Consultant

Rockville, MD · On-site

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

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Valspec

CQV Consultant

Boston, MA

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

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Valspec

CQV Consultant

Holly Springs, NC · On-site

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

Apply Early

Valspec

CQV Consultant

Philadelphia, PA · On-site

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

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Valspec

CQV Consultant

Oceanside, CA · On-site

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100 ...

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Zifo

Principal CQV Consultant

Cary, NC · Hybrid

Identify new qualification/validation opportunities across labs, manufacturing, QC, and QC IT ... Advise and guide onsite/remote validation consultants on qualification strategy, deviations, test ...

Katalyst CRO

CSV Engineer

Redwood City, CA · On-site

Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate ...

Zifo

Principal CQV Consultant

Cary, NC · On-site

Identify new qualification/validation opportunities across labs, manufacturing, QC, and QC IT ... Advise and guide onsite/remote validation consultants on qualification strategy, deviations, test ...

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Jedson Engineering Inc

PR · On-site

Location: south-east of the island Qualifications • Bachelor in Engineering or science and over 5 years of experience as validation consultant and/or Project Manager in regulated industry. • ...

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Validation Consultant information

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How much do validation consultant jobs pay per hour?

As of Jul 5, 2026, the average hourly pay for validation consultant in the United States is $58.47, according to ZipRecruiter salary data. Most workers in this role earn between $51.44 and $65.14 per hour, depending on experience, location, and employer.

How does a Validation Consultant typically collaborate with cross-functional teams during a project?

Validation Consultants frequently work alongside quality assurance, engineering, and regulatory teams to ensure processes and products meet industry standards. They participate in meetings to clarify requirements, coordinate testing schedules, and address compliance issues. Effective communication and documentation are key, as they must translate technical validation findings into actionable information for both technical and non-technical stakeholders. This collaborative approach is essential to streamline project timelines and maintain regulatory compliance.

What is the difference between Validation Consultant vs Quality Assurance Specialist?

AspectValidation ConsultantQuality Assurance Specialist
CredentialsOften requires certifications like GxP, CSV, or industry-specific validation trainingTypically holds certifications in QA, ISO standards, or industry-specific quality management
Work EnvironmentWorks mainly in regulated industries like pharmaceuticals, biotech, or medical devices, focusing on validation processesWorks across various industries ensuring product and process quality, often in manufacturing or service sectors
Employer & Industry UsageCommonly employed by pharmaceutical, biotech, and medical device companies for validation projectsEmployed broadly in manufacturing, software, healthcare, and other sectors for quality oversight

While both roles focus on quality and compliance, Validation Consultants specialize in validation processes for regulated industries, ensuring systems and equipment meet standards. Quality Assurance Specialists oversee overall quality systems and compliance across various sectors. The roles often overlap but differ mainly in scope and industry focus.

What are the key skills and qualifications needed to thrive as a Validation Consultant, and why are they important?

To thrive as a Validation Consultant, you need expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and a relevant science or engineering degree. Familiarity with validation lifecycle documentation, risk assessment tools, and systems like GMP software is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top candidates apart in this role. These skills are crucial for ensuring product quality, regulatory adherence, and smooth project execution within highly regulated industries.

What is the highest paid type of consultant?

Among consulting roles, management consultants, especially those specializing in strategy or executive advisory, tend to earn the highest salaries. Validation consultants typically earn less than specialized management or IT consultants, whose expertise in areas like cybersecurity or digital transformation commands higher compensation.

How to become a validation specialist?

To become a validation specialist, typically one needs a background in science, engineering, or a related field, along with knowledge of validation processes in regulated industries such as pharmaceuticals or manufacturing. Gaining experience with Good Manufacturing Practices (GMP), validation protocols, and relevant tools is essential. Certifications like the Certified Quality Auditor (CQA) or Validation Certification can enhance job prospects.

What does a validation consultant do?

A validation consultant evaluates and documents that systems, processes, or equipment meet specified standards and regulatory requirements, often in industries like pharmaceuticals, biotech, or manufacturing. They develop validation protocols, perform testing, and ensure compliance with guidelines such as GMP or FDA regulations, frequently using validation tools and documentation practices.

What Is a Validation Consultant?

A validation consultant advises a company or manufacturer on how to set up a new production project. Their job duties include testing the quality of the process, ensuring that all industry standards are met, and providing recommendations on how to set up the project efficiently. Qualifications for this career typically include a bachelor’s degree in electrical or mechanical engineering and prior job experience. Strong verbal and written communication skills, in addition to a background in analytical problem-solving and knowledge of budgeting and finance are important for success in a validation consultant role.

How much does a validation engineer make at Pfizer?

A validation engineer at Pfizer typically earns between $70,000 and $100,000 annually, depending on experience, location, and certifications. The role involves ensuring compliance with industry standards and often requires knowledge of GMP, validation protocols, and relevant regulatory guidelines.

What is a Validation Consultant?

A Validation Consultant is a professional who specializes in ensuring that processes, systems, or products in industries like pharmaceuticals, biotechnology, or manufacturing meet regulatory standards and function as intended. They design and execute validation protocols, review documentation, and help companies comply with industry regulations such as FDA or EMA guidelines. Validation Consultants often work on projects involving equipment qualification, process validation, and software validation to ensure quality and compliance. Their expertise helps organizations avoid costly errors and regulatory issues. They may work independently or as part of a consulting firm.
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Validation Consultant jobs near you
CQV Consultant

CQV Consultant

Valspec

Collegeville, PA

Full-time

Medical, Retirement

Posted 4 days ago

Be an early applicant

Job description

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

CQV Consultant – Upstream / Downstream / CIP / PSE / Clean Utilities

Location: Holly Springs (100% Onsite)
Type: Long-Term Contract
Start Date: ASAP

Overview We are seeking experienced CQV Consultants to support a major biopharmaceutical manufacturing project in Holly Springs, NC. This is a long-term onsite opportunity supporting commissioning, qualification, and validation activities across multiple process and utility systems in a GMP manufacturing environment. We are specifically looking for strong "A+" level consultants with hands-on pharmaceutical or biotech project experience supporting large-scale manufacturing operations.

We are hiring CQV professionals with experience in one or more of the following areas:

  • Upstream Processing
  • Downstream Processing
  • CIP (Clean-in-Place) Systems
  • PSE (Process Support Equipment)
  • Clean Utilities

Key Responsibilities

  • Execute CQV lifecycle activities including commissioning, IQ/OQ, and field verification
  • Support startup and qualification of GMP manufacturing equipment and utility systems
  • Author, review, and execute validation documentation and protocols
  • Coordinate with engineering, operations, quality, automation, and project teams
  • Support deviation investigations, change controls, and CAPA activities
  • Ensure compliance with GMP, FDA, and regulatory requirements
  • Participate in walkdowns, system turnover, and punch-list resolution
  • Maintain accurate documentation in accordance with data integrity and quality standards

Qualifications

  • Prior CQV experience in pharmaceutical, biotech, or GMP-regulated manufacturing environments
  • Strong knowledge of commissioning and qualification processes
  • Experience supporting one or more of the following: Upstream, Downstream, CIP, PSE, or Clean Utilities systems
  • Familiarity with GMP documentation practices and regulatory requirements
  • Ability to work onsite in Holly Springs, NC on a full-time basis
  • Strong communication and cross-functional collaboration skills

Preferred Experience

  • Large-scale biologics or vaccine manufacturing projects
  • Startup or greenfield facility experience
  • Experience with DeltaV, MES, or automated process systems
  • Knowledge of clean utilities including WFI, clean steam, compressed gases, and purified water systems

Why Join Valspec?

At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including:

  • Premium medical coverage
  • 401(k) with company match
  • Tuition reimbursement
  • Unique performance incentives
  • And more — all designed to support your growth, well-being, and future.

Join a team where your contributions matter, your development is prioritized, and your success is shared.

When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored.

Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.

Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.

Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.