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Pharma Validation Engineer Jobs (NOW HIRING)

August Bioservices

Validation Engineer

Nashville, TN

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... August Bioservices is looking for a Validation Engineer team member that is passionate and driven ...

Apply Early

August Bioservices

Validation Engineer

Nashville, TN · On-site

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... August Bioservices is looking for a Validation Engineer team member that is passionate and driven ...

August Bioservices

Validation Engineer

Nashville, TN · On-site

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... August Bioservices is looking for a Validation Engineer team member that is passionate and driven ...

Algo Soft Solutions LLC

Pharma CQV Lead

Harvard, MA · On-site

We are seeking a Lead CQV Engineer / CQV Project Manager to serve as the primary CQV technical lead ... or validation lead experience • Strong experience with equipment qualification, protocol ...

Intellectt INC

Mold Validation Engineer

Grand Rapids, MI · On-site

Mold Validation Engineer Locations: Grand Rapids, MI / Dexter, MI / Minneapolis, MN Role Summary ... Experience in regulated industry (Medical Device/Pharma) * Strong expertise in IQ/OQ/PQ, DOE, and ...

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Tekhawks LLC

Be Seen First

Validation Engineer - (Medical Device, Pharma)

Jacksonville, FL · On-site

$35 - $40/hr

Validation Engineer Location: Jackson, FL Duration: 1.5-year contract Hours per week: 40+ We are seeking two mid-level Validation Engineers to support a large capital expansion at a leading medical ...

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Tekhawks LLC

Be Seen First

Validation Engineer - (Medical Device, Pharma)

Jacksonville, FL · On-site

$35 - $40/hr

Validation Engineer Location: Jackson, FL Duration: 1.5-year contract Hours per week: 40+ We are seeking two mid-level Validation Engineers to support a large capital expansion at a leading medical ...

Catalent, Inc.

Validation Engineer

Chelsea, MA · On-site

$89K - $110K/yr

The Validation Engineer is responsible for executing validation activities within a GMP ... Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or ...

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Senior Validation Engineer Location: Portsmouth, NH - 03801 Duration: 7 Months Job Type: Temporary ... Prior experience leading or supporting projects in Biotech, Pharma, or Biologics industries

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adareps

Validation Engineer

Vandalia, OH

Our Business Adare Pharma Solutions is a global Contract Development and Manufacturing Organization ... Position Validation Engineer Location Vandalia, Ohio Summary In this position, the Engineer will ...

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Pharma Validation Engineer information

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How much do pharma validation engineer jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for pharma validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What does a typical day look like for a Pharma Validation Engineer?

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

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 job?

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.

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Pharma Validation Engineer jobs near you
Validation Engineer

Validation Engineer

August Bioservices

Nashville, TN

Full-time

Posted 8 days ago

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Job description

Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO).  As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project – including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!

August Bioservices is looking for a Validation Engineer team member that is passionate and  driven regarding their work. August Bioservices is in need of a motivated individual to provide their expertise in the delivery of results for the company and its clients.
 
Reporting to the Supervisor of Validation, the Validation Engineer will be responsible for performing validation related tasks for the Nashville site. The Validation Engineer independently performs validation tasks to serve company and customer needs and to be in compliance with cGMPs.  
 
 
 
Responsibilities
  • Prepares validation protocols (IQ/OQ/PQ) and final reports for equipment and processes;
  • Oversees validation and revalidation studies for protocol compliance;
  • Develops validation acceptance criteria;
  • Performs validation fieldwork on an as-needed basis;
  • Writes and revises Standard Operating Procedures (SOPs);
  • Recommends validation procedural and test improvements;
  • Plan, track, and perform validation projects;
  • Maintain current validation project schedules;
  • Provide training for contract validation personnel;
  • Review critical equipment drawings from a Validation perspective;
  • Review and summarize equipment history files to assess the validated state of equipment;
  • Proactively identifies potential obstacles to successful project completion. Establishes remediation plans to overcome these obstacles; and
  • Participates as validation representative on failure investigation teams.
Requirements
  • •BS in Biology, Biochemistry, Biotechnology, Microbiology, Chemical Engineering, Mechanical Engineering, Pharmaceutical Engineering or other related discipline.
  • Excellent verbal and written communication skills
  • Preferred Qualifications:
  • 2-5 years of experience with BS in Pharmaceutical, Biological or Biotech industry; hands-on experience in manufacturing operations or pilot lab / scale-up operations
At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule – from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.
 
We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!

August Bioservices  is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.