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Pharmaceutical Validation Manager Jobs (NOW HIRING)

GSK

Validation Standards Manager

Hamilton, MT · On-site

... years of pharmaceutical or biopharmaceutical validation experience. * Experience leading or ... Certification or demonstrated experience in project management or risk management. * Experience ...

Guerbet

Mgr Quality Validation

Raleigh, IL · On-site

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals ... Responsible for managing the development and the execution of qualifications, validations, re ...

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Pharmaceutical Validation Manager information

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$47.5K

$105.4K

$160.5K

How much do pharmaceutical validation manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for pharmaceutical validation manager in the United States is $105,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $132,000.00 per year, depending on experience, location, and employer.

What does a pharmaceutical validation manager do?

A Pharmaceutical Validation Manager oversees the validation processes for equipment, systems, and processes within pharmaceutical manufacturing to ensure compliance with regulatory standards such as FDA and EMA guidelines. Their responsibilities include planning, coordinating, and documenting validation activities, managing teams, and ensuring that products meet quality and safety requirements. They play a key role in ensuring that all manufacturing procedures consistently produce products that meet predetermined quality criteria. Additionally, they may liaise with regulatory agencies during inspections and audits.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation manager?

To thrive as a Pharmaceutical Validation Manager, you need a solid background in pharmaceutical sciences, engineering, or a related field, often supported by a relevant degree and experience in GMP-regulated environments. Familiarity with validation lifecycle documentation, risk assessment tools, and regulatory software systems such as TrackWise or Veeva Vault is typically required. Strong leadership, problem-solving, and communication skills set outstanding managers apart, enabling them to lead cross-functional teams and ensure compliance. These skills and qualities are crucial for maintaining product quality, meeting regulatory standards, and ensuring the safe and efficient production of pharmaceuticals.

What are some common challenges faced by pharmaceutical validation managers during regulatory inspections?

Pharmaceutical Validation Managers often encounter challenges during regulatory inspections, such as ensuring all validation documentation is complete, up-to-date, and compliant with current Good Manufacturing Practices (cGMP). Another challenge is demonstrating that all equipment and processes consistently operate within specified parameters, especially when inspectors request traceability and data integrity. Being able to quickly and accurately address auditor questions, provide supporting evidence, and manage unexpected findings requires thorough preparation and strong organizational skills.
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Pharmaceutical Validation Manager jobs near you
Infographic showing various Pharmaceutical Validation Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.

Validation Project Lead / Documentation Audit Lead

FST Technical Services

Durham, NC • On-site

Full-time

Re-posted 4 days ago

Job description


Validation Project Lead / Documentation Audit LeadMajor Pharmaceutical Facility Construction Project
Location: Durham, NC - FST Life Science office
FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical manufacturing facility construction project.
This role is responsible for establishing a standardized process for the validation of hygienic welding documentation (Isometrics) to ensure compliance with project specifications, applicable codes (e.g., ASME BPE), and industry best practices to support full traceability for hygienic systems..
Responsibilities
  • Lead documentation audit activities to ensure full traceability of hygienic piping systems.
  • Manage schedule, priorities, milestones, and deliverables.
  • Audit weld documentation packages for GMP and Good Documentation Practices (GDP) compliance.
  • Ensure document traceability.
  • Coordinate resolution of documentation deficiencies and quality observations.
  • Partner with Construction Management, Fabricators and Client representatives.
  • Maintain validation metrics and documentation status reports.
  • Mentor junior validation specialists and documentation specialists.
Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related technical discipline (or equivalent experience).
  • 8+ years of pharmaceutical validation, CQV, QA, or GMP documentation experience.
  • 3+ years leading validation documentation or CQV teams on large pharmaceutical capital projects.
  • Strong knowledge of FDA cGMP regulations (21 CFR Parts 210 & 211).
  • Thorough understanding of Good Documentation Practices (GDP).
  • Experience supporting Commissioning, Qualification & Validation activities.
  • Experience preparing projects for client and regulatory audits.
  • Excellent project management, organization, and communication skills.
Preferred Qualifications
  • Experience with Traceability Matrices, ALCOA+, Equipment & Utilities Installation Qualification,
Experience with EIDA, Bluebeam, Microsoft Office and SharePoint.

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