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Validation Engineer Entry Level Jobs in Ohio (NOW HIRING)

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

They are seeking an Entry Level SAS Programmer to join their Biostatistics team, where the ... validate and maintain mapped database • Program edit checks for external data • Coordinate ...

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

Entry Level SAS Programmer Our corporate activities are growing rapidly, and we are currently ... Using SAS, program, validate and maintain mapped database * Program edit checks for external data

GPD Group

Entry-Level Civil Engineer

Akron, OH

Entry-Level Civil Engineer Join GPD Group, where our purpose is to improve the well-being of our ... Valid Driver's License is required. Day-to-day job responsibilities: * Site planning and ...

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Validation Engineer Entry Level information

What engineer makes $500,000 a year?

While most entry-level validation engineers do not earn that level of salary, senior validation engineers or those in highly specialized industries such as pharmaceuticals or aerospace can reach or exceed $500,000 annually with bonuses and stock options. These roles typically require extensive experience, advanced certifications, and expertise in regulatory compliance and validation processes.

What is a Validation Engineer Entry Level job?

An Entry-Level Validation Engineer is responsible for testing and verifying that products, systems, or processes meet required standards and specifications. They work in industries like pharmaceuticals, manufacturing, and software, ensuring compliance with regulations and quality standards. Their tasks may include writing test protocols, analyzing data, and troubleshooting issues. This role requires attention to detail, problem-solving skills, and knowledge of engineering principles. Typically, they work under supervision but gain experience to take on more complex validation tasks over time.

Is QA engineer entry-level?

A QA engineer entry-level position typically involves basic testing and quality assurance tasks, often requiring little to no prior experience. It is suitable for recent graduates or those new to the field, and may involve learning testing tools and methodologies. Advancement usually requires gaining experience and developing skills in automation, scripting, or specific testing environments.

Are validation engineers in demand?

Validation engineers are in demand across industries such as pharmaceuticals, biotechnology, and manufacturing, where compliance with quality standards is essential. The role often requires knowledge of regulatory requirements, validation protocols, and tools like GxP and SOPs, making skilled professionals valuable in ensuring product quality and safety.

How to get into validation engineering?

To enter validation engineering, candidates typically need a bachelor's degree in engineering, science, or a related field. Gaining experience with quality systems, validation protocols, and tools like GMP or GLP is important, along with developing skills in documentation and regulatory compliance. Certifications such as CQE or CSQE can enhance prospects in this field.

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

To thrive as a Validation Engineer Entry Level, you need a solid background in engineering or the life sciences, attention to detail, and a basic understanding of validation protocols and regulatory standards. Familiarity with technical tools such as data logging software, validation documentation, and quality management systems like ISO or GMP is highly valuable. Strong analytical thinking, problem-solving, and effective communication are crucial soft skills for collaborating with multidisciplinary teams and presenting findings. These abilities ensure accuracy, compliance, and effective teamwork in delivering reliable processes and products in regulated industries.

What are the typical daily responsibilities of an Entry Level Validation Engineer?

As an Entry Level Validation Engineer, your daily tasks often include executing validation protocols, documenting test results, and assisting with equipment or process qualification under supervision. You'll collaborate closely with senior engineers, quality assurance teams, and production staff to ensure systems meet regulatory and company standards. Troubleshooting, process improvement, and maintaining accurate records are also common parts of the role. This position is a great opportunity to develop technical expertise and gain practical experience in a regulated industry, setting the foundation for future career advancement.

What are the most commonly searched types of Validation Engineer jobs in Ohio? The most popular types of Validation Engineer jobs in Ohio are:
What are popular job titles related to Validation Engineer Entry Level jobs in Ohio? For Validation Engineer Entry Level jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Validation Engineer Entry Level jobs in Ohio look for? The top searched job categories for Validation Engineer Entry Level jobs in Ohio are:
What cities in Ohio are hiring for Validation Engineer Entry Level jobs? Cities in Ohio with the most Validation Engineer Entry Level job openings:
Validation Engineer Entry Level jobs near you
Infographic showing various Validation Engineer Entry Level job openings in Ohio as of June 2026, with employment types broken down into 3% As Needed, 88% Full Time, 6% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.
SAS Programmer - Entry Level

SAS Programmer - Entry Level

Medpace

Cincinnati, OH • On-site

Full-time

Posted 6 days ago

Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

12th of 58 rated research

Job description

Job Summary:
Medpace is a full-service clinical contract research organization that provides Phase I-IV clinical development services. They are seeking an Entry Level SAS Programmer to join their Biostatistics team, where the candidate will write SAS programs and coordinate communication regarding database specifications.
Responsibilities:
• Write SAS programs for use in creating analysis datasets, tables, listings, and figures
• Using SAS, program, validate and maintain mapped database
• Program edit checks for external data
• Coordinate communication and issues with Data Management regarding database specifications and data transfers
Qualifications:
Required:
• BS in Statistics, Mathematics, Life Sciences, or related field
• SAS Programming experience required
• Minimum 3.4 GPA
Company:
Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology Founded in 1992, the company is headquartered in Cincinnati, USA, with a team of 5001-10000 employees. The company is currently Late Stage.

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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