ZipRecruiter

Log In

1

Pharmaceutical Validation Analyst Jobs (NOW HIRING)

Actalent

Validation Specialist

Oklahoma City, OK

Manage the lifecycle of computerized systems in a regulated pharmaceutical manufacturing ... Conduct risk assessments, gap analyses, and traceability exercises to identify and mitigate ...

New

Alcami Corporation

Sr. Validations Specialist

Morrisville, NC · On-site

$77K - $106K/yr

... general pharmaceutical validation of equipment and GxP computerized systems. Specific ... The ideal candidate will work on extremely complex problems in which analysis of situations or data ...

previous page

Showing results 41-60

All JobsHealthcare JobsMedical Specialists JobsClinical Pharmacist JobsPharmaceutical Validation Analyst Jobs

Pharmaceutical Validation Analyst information

See salary details

$35K

$75.5K

$131K

How much do pharmaceutical validation analyst jobs pay per year?

As of Aug 21, 2026, the average yearly pay for pharmaceutical validation analyst in the United States is $75,517.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $89,500.00 per year, depending on experience, location, and employer.

What is a pharmaceutical validation analyst?

Pharmaceutical Validation Analysts are professionals responsible for ensuring that processes, equipment, and systems used in the production of pharmaceuticals meet regulatory standards and function as intended. They design and execute validation protocols, perform risk assessments, and document results to guarantee product quality and safety. Their work is essential for regulatory compliance and helps prevent errors that could impact patient health. Validation analysts often collaborate with quality assurance, manufacturing, and engineering teams to maintain consistent standards throughout the production process.

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

To thrive as a Pharmaceutical Validation Analyst, you need a strong background in pharmaceutical sciences, quality assurance, and regulatory compliance, often supported by a relevant degree in life sciences or engineering. Familiarity with validation protocols, Good Manufacturing Practice (GMP) standards, and software such as LIMS or TrackWise is commonly required. Attention to detail, analytical thinking, and effective communication are essential soft skills for success in this role. These skills and qualifications are crucial to ensure that pharmaceutical products meet regulatory requirements, maintain safety standards, and pass rigorous quality checks.

What are some common challenges faced by pharmaceutical validation analysts during equipment qualification projects?

Pharmaceutical Validation Analysts often encounter challenges such as tight project timelines, evolving regulatory requirements, and the need to coordinate with multiple departments—including manufacturing, quality assurance, and engineering. Ensuring that all equipment meets stringent validation standards while minimizing downtime can be demanding. Effective communication, meticulous documentation, and adaptability are crucial for managing these complexities and delivering successful outcomes.

What is the difference between Pharmaceutical Validation Analyst vs Quality Control Analyst?

AspectPharmaceutical Validation AnalystQuality Control Analyst
CredentialsBachelor's in Life Sciences, Validation certificationsBachelor's in Chemistry, Quality certifications
Work EnvironmentValidation labs, manufacturing facilitiesQC labs, manufacturing sites
Industry UsageValidation of processes, equipment, systemsTesting products, ensuring quality standards

The Pharmaceutical Validation Analyst focuses on validating processes and equipment to ensure compliance with industry standards, while the Quality Control Analyst primarily tests products to verify quality and safety. Both roles are essential in pharmaceutical manufacturing, often working closely but with distinct responsibilities.

More about Pharmaceutical Validation Analyst jobs

What job categories do people searching Pharmaceutical Validation Analyst jobs look for?

The top searched job categories for Pharmaceutical Validation Analyst jobs are:

Pharmaceutical Validation Analyst jobs near you
Infographic showing various Pharmaceutical Validation Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $75,517 per year, or $36.3 per hour.

Validation Engineer

Validation & Engineering Group, Inc.

New Albany, OH • On-site

Full-time

Re-posted 7 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) 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:
The role demands deep technical expertise across the full validation lifecycle � including URS development, FAT/SAT execution, and Computer System Validation (CSV) � as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.
Key Responsibilities:
  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:
  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

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.

Apply