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Entry Level Pharmaceutical Validation information

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How much do entry level pharmaceutical validation jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for entry level pharmaceutical validation in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.

What is an entry level pharmaceutical validation specialist?

Entry level pharmaceutical validation jobs involve ensuring that pharmaceutical products, processes, and equipment meet regulatory standards and operate as intended. Individuals in these roles typically assist with the documentation, testing, and qualification of manufacturing equipment and procedures. They work closely with quality assurance and production teams to ensure compliance with Good Manufacturing Practices (GMP) and FDA regulations. These positions are ideal for recent graduates in life sciences or engineering fields who are looking to start a career in the pharmaceutical industry.

What are the key skills and qualifications needed to thrive as an entry level pharmaceutical validation specialist?

To thrive as an Entry Level Pharmaceutical Validation Specialist, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory requirements such as GMP. Familiarity with validation protocols, data analysis software, and documentation systems is commonly expected, along with relevant training or certifications in pharmaceutical processes. Attention to detail, problem-solving abilities, and effective communication help you excel in cross-functional teams and ensure accuracy. These competencies are critical for maintaining product quality, regulatory compliance, and the integrity of pharmaceutical manufacturing processes.

What are some typical challenges faced by entry-level professionals in pharmaceutical validation, and how can they be addressed?

Entry-level professionals in pharmaceutical validation often face challenges such as understanding complex regulatory standards (like FDA or EMA guidelines), adapting to rapidly changing project requirements, and managing detailed documentation. These challenges can be addressed by seeking mentorship from experienced colleagues, actively participating in training sessions, and consistently reviewing standard operating procedures. Building strong communication skills is also crucial, as validation specialists frequently collaborate with quality assurance, manufacturing, and engineering teams to ensure compliance and resolve issues efficiently.

What is the difference between Entry Level Pharmaceutical Validation vs Quality Control Technician?

AspectEntry Level Pharmaceutical ValidationQuality Control Technician
Required CredentialsBachelor's in Life Sciences, GMP knowledge, Validation certifications (if any)Associate's or Bachelor's in Science, GMP familiarity, QC certifications (if any)
Work EnvironmentManufacturing facilities, validation labs, regulated environmentsLaboratories, manufacturing sites, quality testing areas
Employer & Industry UsagePharmaceutical companies, biotech firms, contract manufacturingPharmaceutical, biotech, and medical device industries
Common Search & ComparisonYesYes

Entry Level Pharmaceutical Validation focuses on ensuring equipment, processes, and systems meet regulatory standards through validation procedures. Quality Control Technicians primarily perform testing and inspections to verify product quality. While both roles operate within pharmaceutical manufacturing and require GMP knowledge, validation roles emphasize process validation, whereas QC roles focus on product testing. Understanding these differences helps job seekers identify the right career path in the pharmaceutical industry.

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Entry Level Pharmaceutical Validation jobs near you
Infographic showing various Entry Level Pharmaceutical Validation job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $104,945 per year, or $50.5 per hour.

Entry Level Validation Engineer

Barry-Wehmiller

Fort Worth, TX • On-site

$75K - $90K/yr

Full-time

Posted 3 days ago

New

Job description

About Us:

BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.


 

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.


 

Job Description:

Who You'll Work With

At Design Group,you'llcollaborate with experienced leaders, technical specialists, and subject matter experts to solve complex challenges for some of the world's leading companies.You'lljoin a growing team of more than 1,500 professionals across 45 U.S. offices whereyou'llbe empowered to make an impact, develop yourexpertise, and grow your career.

What You'll Do

In this role,you'llbe responsible forsupporting validation and regulatory compliance activities for pharmaceutical, medical device, and other life sciences projects.You'llwork closely with validation engineers, project teams, clients, vendors, and technical specialists to develop protocols, execute testing, investigate issues, and document results. This position playsan important rolein helping clientsdemonstratethat equipment, utilities, facilities, and automated systems meet quality and regulatory requirements while giving you hands-on experience invalidationengineering and project delivery.

  • Develop and execute validation and FDA compliance documents and protocols for pharmaceutical equipment and automated systems

  • Support manufacturing process design, facility development, and project execution activities

  • Prepare and execute FAT, SAT, IQ, and OQ documentation for equipment and automated systems

  • Assistwith development and execution of quality management system procedures and related compliance documentation

  • Apply applicable requirements from 21 CFR Parts 211 and 820 and ICH Q1, Q8, Q9, and Q10 to project deliverables

  • Conduct investigations and support troubleshooting of validation and compliance issues

  • Prepare clear written validation reports that document testing, results, deviations, and conclusions

  • Coordinate with clients, vendors, engineers, and project teams to support validation planning and execution

  • Support installation, start-up, commissioning, and site-based validation activities

  • Build technicalexpertisein life sciences validation, quality systems, documentation practices, and regulatory compliance

What You'll Bring

Qualifications

  • Bachelor of Science in bioengineering, biomedical engineering, chemical engineering, or a related technical degree

  • Academic, co-op, internship, project, or entry-level experience related to validation, quality, pharmaceutical manufacturing, medical devices, automation, utilities, facilities, or regulated environments

  • Proficiencyusing Microsoft Office and ability to prepare clear technical documentation

  • Ability to organize and execute multiple project responsibilities simultaneously

  • Ability to travel for project requirements, including installation and start-up activities, client and company meetings, trainings, seminars, forums, and conventions

Preferred Qualifications

  • Co-op or project experience with validation of automation, packaging equipment, utilities, or facilities

  • Co-op or project experience in pharmaceutical or medical device environments

  • Exposure to FAT, SAT, IQ, OQ, quality systems, FDA requirements, or technical report writing

Compensation

The approximate pay range for this position is$75,000-$90,000. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities, as well as geographic location of the position.


 

At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.


 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.


Company:

Design Group

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