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Pharma Validation Engineer Jobs in Georgia (NOW HIRING)

Intellectt INC

CSV Engineer

Social Circle, GA · On-site

CSV Engineer I Location: Social Circle, Georgia, USA Duration: Longterm Job Summary The CSV ... Basic knowledge of CSV, CQV, GMP, and validation lifecycle . * Understanding of pharma regulations ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

PROLIM Global Corporation

Lead Design Engineer

Duluth, GA · On-site

$94K - $124K/yr

Lead Design Engineer - PAS-X MES Location: Duluth, Georgia (Onsite/Hybrid - as per client ... in Pharma, Biotech, or Life Sciences environments * Solid understanding of MES validation ...

LTTS

Mechanical Engineer

Atlanta, GA · On-site

Create and validate equipment, master data and asset attributes. * Establish equipment hierarchy ... Experience: 5-7 years in Process / Packaging plants (FMCG / Pharma / Food) including Asset ...

Sparus

Project Manager

Peachtree Corners, GA · On-site

... Validation. Have responsibilities related to the planning, design, and implementation of ... engineering pharma project interests on collaborative teams for pharmaceutical manufacturing ...

The Spear Group

Project Manager

Peachtree Corners, GA · On-site

... Validation. Have responsibilities related to the planning, design, and implementation of ... engineering pharma project interests on collaborative teams for pharmaceutical manufacturing ...

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Pharma Validation Engineer information

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$43

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How much do pharma validation engineer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for pharma validation engineer in Georgia is $43.90, according to ZipRecruiter salary data. Most workers in this role earn between $33.27 and $53.37 per hour, depending on experience, location, and employer.

What does a pharma validation engineer do?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.

What skills and qualifications are needed to be a pharma validation engineer?

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

What is a pharma validation engineer?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

What are popular job titles related to Pharma Validation Engineer jobs in Georgia? For Pharma Validation Engineer jobs in Georgia, the most frequently searched job titles are:
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Pharma Validation Engineer jobs near you
Infographic showing various Pharma Validation Engineer job openings in Georgia as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $91,322 per year, or $43.9 per hour.

Senior Process Validation Engineer

Chemence

Alpharetta, GA • On-site

Full-time

Re-posted 9 days ago

Job description

Summary:

Key Duties and Responsibilities:

Chemence Medical Inc. seeks Sr. Process Validation Engineer in Alpharetta, GA to develop IQ/OQ/PQ protocols, coordinate and perform equipment qualifications, and ensure that automated process equipment that mass produce medical device consumables and other products, are designed, developed, or changed in compliance with specifications, requirements, safety, and Company and regulatory guidelines. The Sr. Process Validation Engineer will work closely with engineering, operations, and R&D teams to create and document procedures to validate products and processes.

Qualifications, Education and/or Experience Required:

  • Must have a Bachelor's degree in Mechanical Engineering or a related Life Science/Engineering discipline.
  • Must have 3 years’ experience in Validation Engineering, including experience developing Installation Qualification/Operational Qualification/Performance Qualification (IQ/OQ/PQ) validation/qualification protocols for equipment within an FDA regulated pharma, medical device, or biotech industry.