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Pharmaceutical Validation Jobs (NOW HIRING)

Argenta

Validation Specialist

Shawnee, KS · On-site

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated ...

Argenta

Validation Specialist

Shawnee, KS

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated ...

Pfizer

Sr. Manager, Validations

Mcpherson, KS

Strong technical expertise in GMP validation and qualification within aseptic pharmaceutical manufacturing. Demonstrated expertise in aseptic processing validation, including APS/media fills ...

Pfizer, Inc.

Sr. Manager, Validations

Mcpherson, KS · On-site

Strong technical expertise in GMP validation and qualification within aseptic pharmaceutical manufacturing. Demonstrated expertise in aseptic processing validation, including APS/media fills ...

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Pharmaceutical Validation information

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$22

$51

$78

How much do pharmaceutical validation jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for pharmaceutical 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 are the 4 types of validation in pharma?

In pharmaceutical validation, the four main types are Installation Qualification (IQ), which verifies equipment setup; Operational Qualification (OQ), which confirms equipment functions correctly; Performance Qualification (PQ), which ensures processes produce consistent results; and Process Validation, which demonstrates that manufacturing processes are effective and reproducible. These validation types are essential for ensuring product quality and compliance with regulatory standards in the pharma industry.

What is the role of validation in pharmaceutical industry?

In pharmaceutical validation, the role is to ensure that manufacturing processes, equipment, and systems consistently produce products that meet quality standards and regulatory requirements. Validation helps identify and control potential risks, supporting compliance with Good Manufacturing Practices (GMP) and ensuring product safety and efficacy. It involves activities such as process validation, equipment qualification, and cleaning validation, often requiring documentation and testing to verify performance.

What are some of the main challenges encountered in a Pharmaceutical Validation role?

One of the main challenges in Pharmaceutical Validation is staying updated with constantly evolving regulatory requirements and ensuring that all validation activities meet stringent compliance standards. Professionals often manage multiple concurrent projects, which requires effective prioritization, organization, and close coordination with cross-functional teams such as quality assurance, manufacturing, and engineering. Thorough documentation and meticulous attention to detail are essential, as even minor oversights can lead to compliance issues. However, overcoming these challenges provides valuable problem-solving experience and opportunities for advancement within quality assurance, regulatory affairs, or project management.

What is a Pharmaceutical Validation job?

A Pharmaceutical Validation job involves ensuring that systems, equipment, and processes in the pharmaceutical industry meet regulatory and quality standards. Professionals in this role develop protocols, conduct testing, and document validation activities to ensure compliance with regulations like FDA, EU GMP, and ISO standards. They work with manufacturing processes, laboratory instruments, and software to verify that products are consistently produced and controlled according to required quality standards. This role is critical in maintaining drug safety, efficacy, and regulatory approval.

What is the highest paying job in the pharma industry?

In pharmaceutical validation, senior roles such as Validation Director or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and FDA requirements.

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

To thrive in Pharmaceutical Validation, you need a strong background in pharmaceutical sciences or engineering, familiarity with regulatory guidelines (such as FDA, GMP, and ICH), and hands-on experience in validation protocols. Proficiency with validation lifecycle documentation tools, quality management systems (QMS), and specialized software like TrackWise or ValGenesis is essential. Attention to detail, analytical thinking, and excellent collaboration and communication skills are highly valued in this role. These competencies ensure that pharmaceutical processes, equipment, and systems meet strict quality standards, supporting product safety and regulatory compliance.

How much does a validation engineer make?

A validation engineer in the pharmaceutical industry typically earns between $70,000 and $100,000 annually, depending on experience, location, and certifications. Salaries can vary based on the complexity of validation tasks and the company's size, with senior roles potentially earning higher compensation.
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Pharmaceutical Validation jobs near you
Validation Engineer

Validation Engineer

Performance Validation, Inc

Raleigh, NC

$80K - $83K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

Job description

About Us
Here at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for 37 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About the job
Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader.
Responsibilities
  • Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements
  • Work in a team environment to meet defined objectives based on established timelines
  • Develop verification/qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports
  • Execute test protocols, including identification and resolution of non-conformances/deviations
  • Track and manage change control activities for multiple concurrent projects

Requirements you will need
Education:
  • BS/BA degree and 1-2 years in pharmaceutical or other regulated industry experience directly related to pharmaceutical validation
  • BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred

Experience:
  • Change and Deviation Management
  • Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees
  • Possess excellent oral and written communication skills and high attention to detail
  • Cleaning, Sterlization, and Decontamination Validation experienced preferred
  • Device Assembly and Packing experience preferred

What we have to offer
  • Competitive base salary
  • Biannual profit share
  • Employee stock ownership program
  • 401(k) company match
  • Flexible time off policy
  • Paid Parental Leave
  • Internal and external training opportunities
  • Medical, vision, and dental coverage
  • Disability and life insurance
  • Cellphone stipend
  • Growth opportunities
  • Company-sponsored team building outings
  • A collaborative work environment
  • Work/life harmony

This role involves frequent travel to client and partner sites, estimated at 30–50% depending on business needs and project cycles.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.

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