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Pharma Validation Jobs (NOW HIRING)

Algo Soft Solutions LLC

Pharma CQV Lead

Harvard, MA · On-site

... or validation lead experience • Strong experience with equipment qualification, protocol ... pharma validation workflows • Experience supporting fast-paced GMP readiness or capacity ...

Biogen

NC · On-site

$111K - $149K/yr

About This Role As a Scientist II within Pharma Validation, Transfer and Registration (VTR), you will serve as a subject matter expert supporting analytical method validation, transfer, investigation ...

Intellectt INC

Validation Lead

Raleigh, NC · On-site

Lead end-to-end validation activities for pharma manufacturing equipment, utilities, facilities, and processes. * Prepare, review, and approve validation documents including DQ, IQ, OQ, PQ, protocols ...

Apply Early

Peregrine Team

Validation Engineer

Philadelphia, PA · On-site

Bachelor's degree in Engineering or related field * 3-5+ years of validation experience in pharma/biotech * Knowledge of cGMP and validation standards * Strong documentation and technical skills

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Pharma Validation information

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$22

$51

$78

How much do pharma validation jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for pharma 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.

What is pharma validation?

Pharma validation is the process of ensuring that pharmaceutical manufacturing processes, equipment, and systems consistently produce products meeting predetermined quality standards and regulatory requirements. This process involves documenting and verifying each step in the manufacturing process to ensure safety, efficacy, and compliance. Validation activities include installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). Proper validation helps minimize risks, ensures patient safety, and is a critical requirement for regulatory approval by agencies like the FDA.

What are the key skills and qualifications needed to thrive in Pharma Validation, and why are they important?

To thrive in Pharma Validation, you need a strong background in pharmaceutical sciences, regulatory compliance, and validation protocols, often supported by a relevant degree such as pharmacy, chemistry, or engineering. Familiarity with validation tools, Good Manufacturing Practice (GMP) guidelines, and quality management systems is essential, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring thorough documentation and collaboration with cross-functional teams. These skills ensure all processes and products meet stringent regulatory standards, safeguarding product quality and patient safety.

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

AspectPharma ValidationQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality departments, production sites
Industry UsageEnsures equipment, processes meet standardsMaintains quality systems, audits

Pharma Validation focuses on verifying that equipment, processes, and systems meet regulatory standards through validation protocols. Quality Assurance Specialists oversee overall quality systems, conduct audits, and ensure compliance. While both roles aim to ensure product quality, Validation is more technical and process-specific, whereas QA Specialists handle broader quality management and compliance activities.

What are some typical challenges faced by professionals in pharma validation, and how can they be addressed?

Pharma validation professionals often encounter challenges such as keeping up with ever-evolving regulatory requirements, managing tight project timelines, and ensuring thorough documentation throughout the validation process. Addressing these challenges requires ongoing training on current Good Manufacturing Practices (cGMP), effective project management skills, and close collaboration with cross-functional teams such as quality assurance and production. Proactively communicating with stakeholders and staying organized can help mitigate risks and ensure compliance.
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Pharma Validation jobs near you
Infographic showing various Pharma Validation job openings in the United States as of June 2026, with employment types broken down into 71% Full Time, and 29% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Pharma CQV Lead

Algo Soft Solutions LLC

Harvard, MA • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking a Lead CQV Engineer / CQV Project Manager to serve as the primary CQV technical lead for project scope. This resource will own CQV execution strategy, deliverable approach, reviewer alignment, documentation quality, deviation strategy, and technical oversight across equipment workstreams.
Lead CQV Engineer Responsibilities:
•    Lead CQV strategy and execution planning for GMP equipment qualification scope
•    Own documentation strategy for URS revisions, readiness checklists, IOQ/PQ protocols, and QSRs
•    Coordinate technical alignment across engineering, CQV, quality, operations, and vendor teams
•    Review and guide CQV deliverables for consistency, completeness, and GMP readiness
•    Support deviation/discrepancy strategy and execution issue resolution
•    Provide technical oversight to CQV leads, senior engineers, and execution resources
•    Support prioritization of Phase 1 and Phase 2 deliverables
•    Partner with the Senior Project Manager on schedule, risks, issues, and change control
Job Requirements:
•    10+ years direct CQV experience in GMP pharmaceutical, biologics, cell therapy, or life sciences environments
•    Prior CQV technical lead, CQV PM, or validation lead experience
•    Strong experience with equipment qualification, protocol generation, execution, deviations, and QSRs
•    Ability to lead documentation generation and technical review
•    Biologics or cell therapy manufacturing experience preferred
•    Experience with CQV standards, ValGenesis, or large pharma validation workflows
•    Experience supporting fast-paced GMP readiness or capacity expansion projects
This role requires the ability to be on-site, full-time in Devens, MA.

Apply