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Pharma Validation Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering, Life Sciences, or related field. * 1-3 years of experience in validation, CQV, or related technical role in a regulated industry (pharma, biotech, or medical devices)

Peregrine Team

Validation Engineer

Philadelphia, PA · On-site

Bachelor's degree in Engineering or related field * 3-5+ years of validation experience in pharma/biotech * Knowledge of cGMP and validation standards * Strong documentation and technical skills

Aequor

Specialist QA - Validation, cGMP

Woburn, MA · On-site

Company Description Engineering Job Title- Specialist QA Location- Woburn, MA Duration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs ...

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Pharma Validation information

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How much do pharma validation jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for pharma validation 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 is pharma validation?

Pharma validation is the process of ensuring that pharmaceutical manufacturing processes, equipment, and systems consistently produce products meeting predetermined quality standards and regulatory requirements. This process involves documenting and verifying each step in the manufacturing process to ensure safety, efficacy, and compliance. Validation activities include installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). Proper validation helps minimize risks, ensures patient safety, and is a critical requirement for regulatory approval by agencies like the FDA.

What are the key skills and qualifications needed to thrive in pharma validation, and why are they important?

To thrive in Pharma Validation, you need a strong background in pharmaceutical sciences, regulatory compliance, and validation protocols, often supported by a relevant degree such as pharmacy, chemistry, or engineering. Familiarity with validation tools, Good Manufacturing Practice (GMP) guidelines, and quality management systems is essential, along with certifications like Six Sigma or Lean Manufacturing being advantageous. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring thorough documentation and collaboration with cross-functional teams. These skills ensure all processes and products meet stringent regulatory standards, safeguarding product quality and patient safety.

What is the difference between Pharma Validation vs Quality Assurance Specialist?

AspectPharma ValidationQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality departments, production sites
Industry UsageEnsures equipment, processes meet standardsMaintains quality systems, audits

Pharma Validation focuses on verifying that equipment, processes, and systems meet regulatory standards through validation protocols. Quality Assurance Specialists oversee overall quality systems, conduct audits, and ensure compliance. While both roles aim to ensure product quality, Validation is more technical and process-specific, whereas QA Specialists handle broader quality management and compliance activities.

What are some typical challenges faced by professionals in pharma validation, and how can they be addressed?

Pharma validation professionals often encounter challenges such as keeping up with ever-evolving regulatory requirements, managing tight project timelines, and ensuring thorough documentation throughout the validation process. Addressing these challenges requires ongoing training on current Good Manufacturing Practices (cGMP), effective project management skills, and close collaboration with cross-functional teams such as quality assurance and production. Proactively communicating with stakeholders and staying organized can help mitigate risks and ensure compliance.
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What states have the most Pharma Validation jobs?

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What job categories do people searching Pharma Validation jobs look for?

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Pharma Validation jobs near you
Infographic showing various Pharma Validation job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 3% Part Time, 1% Temporary, and 7% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Verification & Validation (V&V) Engineer - Medical Devices

Stark Pharma Solutions Inc

Bellevue, WA • On-site

Contractor

Re-posted 11 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Verification & Validation (V&V) Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Role:  Verification & Validation (V&V) Engineer – Medical Devices

Location: Bellevue, WA (Onsite)
Duration: 12 Months
Experience: 5–8 Years

Job Overview

We are seeking an experienced Verification & Validation (V&V) Engineer to support the development and testing of next-generation connected medical devices. This role will focus on system-level verification and validation across wearable devices, embedded software, mobile applications, cloud platforms, and data pipelines, ensuring products meet regulatory, quality, and performance requirements.

Key Responsibilities

  • Develop and execute system-level Verification & Validation (V&V) plans, protocols, and reports.
  • Lead integration planning and testing across wearable devices, embedded systems, mobile applications, cloud platforms, and user portals.
  • Perform system verification for functionality, performance, reliability, safety, and cybersecurity.
  • Develop risk analyses, system models, and mitigation strategies throughout the product lifecycle.
  • Collaborate with hardware, software, and systems engineering teams to troubleshoot and resolve integration issues.
  • Support requirements management, traceability, and compliance with medical device quality standards.
  • Apply systems engineering best practices throughout product development.

Required Qualifications

  • Bachelor's or Master's degree in Electrical, Biomedical, Computer, or Systems Engineering (or related field).
  • 5–8+ years of Verification & Validation or Systems Engineering experience within the Medical Device industry.
  • Experience with connected medical devices involving hardware, embedded software, mobile applications, and cloud platforms.
  • Strong knowledge of system integration, requirements management, risk analysis, and V&V methodologies.
  • Experience developing test plans, protocols, functional test procedures, and validation documentation.
  • Familiarity with medical device regulations and quality systems.
  • Strong troubleshooting, analytical, and cross-functional collaboration skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com