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Validation Analyst Pharma Jobs (NOW HIRING)

MD ยท On-site

Hi, My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our ... Analyze validation data and investigate deviations to ensure compliance with acceptance criteria.

SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and ... analysis, risk assessment and investigation tools and techniques. * Knowledge and experience in ...

SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and ... analysis, risk assessment and investigation tools and techniques. * Knowledge and experience in ...

IL ยท On-site

Hi, My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client ... Investigate deviations, support CAPA implementation, and participate in root cause analysis.

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract ... Validate analytical methods used in the testing of raw materials, intermediate products, final ...

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Validation Analyst Pharma information

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How much do validation analyst pharma jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for validation analyst pharma in the United States is $31.53, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $35.82 per hour, depending on experience, location, and employer.

What is a validation analyst in the pharmaceutical industry?

Validation Analysts in the pharmaceutical industry are professionals responsible for ensuring that processes, equipment, and systems meet regulatory standards and function as intended. They develop and execute validation protocols, analyze data, and document results to demonstrate compliance with FDA and other regulatory requirements. Their work helps ensure the safety, quality, and efficacy of pharmaceutical products by verifying that manufacturing processes produce consistent and reliable outcomes. Validation Analysts often collaborate with engineers, quality assurance teams, and regulatory bodies. Their role is crucial for maintaining product integrity and meeting industry standards.

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

To thrive as a Validation Analyst in pharma, you need a solid background in life sciences or engineering, knowledge of regulatory guidelines (such as GMP, FDA, or EMA), and experience with validation protocols. Familiarity with validation management software, data integrity tools, and documentation systems is often required, along with certifications like Six Sigma or ASQ. Attention to detail, problem-solving, and strong communication skills help ensure effective cross-functional collaboration and compliance. These abilities are crucial for maintaining product quality, regulatory compliance, and patient safety in pharmaceutical operations.

What are some common challenges faced by validation analysts in the pharmaceutical industry, and how can they be addressed?

Validation Analysts in the pharmaceutical sector often encounter challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring cross-functional collaboration between departments like quality assurance and production. Staying current with FDA and EMA guidelines is crucial, as is maintaining detailed records for audits and inspections. Effective communication, continuous professional development, and adopting robust project management tools can help address these challenges and ensure successful validation processes.

What are popular job titles related to Validation Analyst Pharma jobs?

For Validation Analyst Pharma jobs, the most frequently searched job titles are:

Infographic showing various Validation Analyst Pharma job openings in the United States as of June 2026, with employment types broken down into 96% Full Time, and 4% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $65,589 per year, or $31.5 per hour.

Validation Manager - Pharma

Hickory, NC โ€ข On-site

Full-time

Re-posted 16 days ago


Job description

Company Description
Skye Blue Consulting has been engaged to find a Validation Manager for one of our top clients in Western North Carolina. The client is a small (but growing!) pharma firm with competitive salaries, great benefits and is located in the beautiful foothills area.
Job Description
Job Task(s)
โ€ข Manages all aspects of the Validation/Calibration department.
โ€ข Designs and implements systems to assure quality of data processing across multiple study sites.
โ€ข Works with database designers to set up computer systems.
โ€ข Performs routine testing for product release and stability studies.
โ€ข Helps develop lab documents to support compliance with GMP.
โ€ข Performs routine procedures to monitor adherence to guidelines.
Computer Skill(s)
โ€ข Should have knowledge of Database software; Statistical software; Project Management software; Spreadsheet software and Word Processing software.
โ€ข Knowledge of US Pharmacopeia/National Formulary analytic methods: Knowledge of SPC and DOE is desired but not required.
Qualifications
Education Requirements
This position requires the following minimum education:
โ€ข Bachelor's degree (B.A.) from a four year college OR equivalent combination of education and experience. An advanced degree is preferred.
Work Experience Requirements
โ€ข 3-5 years related experience and/or training
Physical Demand(s)
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently required to sit and talk or hear. The employee is occasionally required to stand; walk and use hands to finger, handle, or feel. Specific vision abilities required by this job include close vision and ability to adjust focus.
Additional Information
All your information will be kept confidential according to EEO guidelines.