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Pharmaceutical Validation Analyst Jobs (NOW HIRING)

Southern Research

Senior Validation Analyst

Birmingham, AL

$108K - $109K/yr

Senior Validation Analyst Southern Research + You Discover a career where your work truly matters ... Advanced knowledge of pharmaceutical/CRO industry regulations, standards, and guidelines (GxP, CSV ...

MedImpact

Testing & Validation Analyst II

$38.85 - $48.38/hr

... pharmaceutical and technology related solutions that dramatically improve the value of health care ... Summary The Testing & Validation Analyst II is responsible for ensuring the quality, accuracy, and ...

Argenta

Validation Specialist

Shawnee, KS · On-site

... trend analysis, control charting, and capability studies (Cp/Cpk). Serve as a validation ... Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related ...

Argenta

Validation Specialist

Shawnee, KS · On-site

... trend analysis, control charting, and capability studies (Cp/Cpk). Serve as a validation ... Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related ...

Pfizer

Sr. Manager, Validations

Mcpherson, KS

... analyses of testing results and process anomalies, and writing, reviewing, approving and/or ... Strong technical expertise in GMP validation and qualification within aseptic pharmaceutical ...

New

Quality Agents, LLC

Validation Engineer IV

Rockville, MD · On-site

... pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the ... Review and approve documented test results and maintain records for later analysis. * Assist with ...

Quality Agents

Validation Engineer II

Rockville, MD · On-site

... pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the ... Review and approve documented test results and maintain records for later analysis. * Assist with ...

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Pharmaceutical Validation Analyst information

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How much do pharmaceutical validation analyst jobs pay per year?

As of Jun 12, 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 are Pharmaceutical Validation Analysts?

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

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 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

GXP-Validation Analyst

Futran Tech Solutions Pvt. Ltd.

Chicago, IL • On-site

Full-time

Posted 22 days ago

Job description

Job title: GXP-Validation Analyst;
Location: Chicago/Nearshore CST time
PURPOSE OF THE POSITION
  • Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures
  • Performing Compliance evaluation of procedures and systems wrt equipment, facilities and computerized systems used in GLP, GMP and GCP environments.
  • Coordinate with cross-functional project teams in for deliverables within the agreed timeline.
  • Support development of best practices within the validation group, based on current industry practices and guidelines.
  • Required to be on the site in Chicago, IL or nearshore supporting Chicago time zone

KEY RESPONSIBILITIES
  • Serve as quality representative and compliance resource, directing the application of company standards for internal validation activities, including quality review and approval of project deliverables
  • Using in-depth professional knowledge, provide guidance to employees, external contractors, clinical investigators, and development partners on complex topics related to computer system regulatory requirements, data integrity, and quality systems
  • Direct and train staff on regulatory requirements, quality management processes and procedures, and inspection readiness
  • Conduct periodic assessment activities to ensure systems are operating in a compliant state and foster continuous improvement
  • Collaborate with functional teams to ensure that the integrity of data and information is maintained throughout its lifecycle
  • Quality Assurance/Audits
  • Commensurate with expertise, plan and conduct internal and external audits of technology in use by customer and tool vendors providing computing services
  • Guide functional teams through the deviation/CAPA process to ensure robust investigation, timely action, and meaningful improvements to process
  • Using quality management system tools, analyze audit findings and deviation trends to drive continuous improvement
  • Collaborate with external contractors conducting audits on behalf of customer. This may include co-auditing activities, providing information about company processes, known quality issues, audit scoping expectations, and/or guidance on use of the audit system
  • Conduct or participate in Mock Regulatory Inspection activities and/or provide guidance to functional teams to facilitate inspection readiness
  • Special Projects, Other Responsibilities as assigned

WORK EXPERIENCE & SKILLS
  • Familiarity with GxP systems (POMSnet, Maximo, OSI PI, SampleManager, Empower, Trackwise, ComplianceWire, Antares, Warehouse Serialization Solution, Discoverant)
  • Experience with Kneat (App Change Management), qTest (ALM), & Tosca (automated testing)
  • Knowledge of FDA and European compliance regulations and GAMP guidelines applicable to computer system validation.
  • Familiar with off-the-shelf, configurable, and custom-developed applications validation.
  • Experienced with various technologies and automated systems used in the pharmaceutical industry - Business System (ERP etc), Quality System (Track wise, LIMS etc), PLC or SCADA, Process Control, Laboratory Instrumentation, Data archive/historian, etc
  • Excellent oral and written communication skills in English. Strong expertise and ability to interview and accurately interpret communication requirements of team members.

ACADEMIC & TRADES QUALIFICATIONS
  • Bachelor's degree in engineering / Master's Degree in science.
  • Total 5 years' of relevant validation testing experience with a minimum of 3 years or more experience in Validation testing.
  • Experience in pharmaceutical/biotech manufacturing or testing is an added advantage

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