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Pharma Validation Jobs (NOW HIRING)

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

The role focuses on implementing best practices, supporting site and process improvement projects, and maintaining GMP-compliant validation and quality systems within a regulated Biotech/Pharma ...

Omni Inclusive

Business Analyst - Pharma

Raleigh, NC · On-site

Pharma IT Business Analyst * Proven experience working as a Business Analyst (BA) or Senior ... Partner with Validation teams to support system validation activities and ensure compliance with ...

Brillio

Pharma Product Manager- R01564155

New York, NY · On-site +1

$75 - $80/hr

CSPO Job requirements Role: - Pharma Product Manager Location: - Remote JD:-Pharma domain Software ... Familiarity with cloud native software development, validation, audit readiness, and change control ...

Brillio

Pharma Product Manager- R01564155

New York, NY · On-site +1

$75 - $80/hr

CSPO Job requirements Role: - Pharma Product Manager Location: - Remote JD:-Pharma domain Software ... Familiarity with cloud native software development, validation, audit readiness, and change control ...

Capgemini

Business Analyst- Pharma Industry

Manhattan, NY · On-site

$65K/yr

Partner with QA teams to validate test cases, scenarios, and data accuracy throughout test cycles Required Skills * Mandatory experience in Pharma / Life Sciences , including specialty pharma, healt ...

Zifo

CSV Validation Analyst

Emeryville, CA

Lead or support validation of computerized systems & laboratory instruments, including installation ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

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All JobsPharma Validation Jobs

Pharma Validation information

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$22

$51

$78

How much do pharma validation jobs pay per hour?

As of Jul 6, 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.
More about Pharma Validation jobs
What states have the most Pharma Validation jobs? States with the most job openings for Pharma Validation jobs include:
What job categories do people searching Pharma Validation jobs look for? The top searched job categories for Pharma Validation jobs are:
Pharma Validation jobs near you
Infographic showing various Pharma Validation job openings in the United States as of June 2026, with employment types broken down into 71% Full Time, and 29% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Senior Validation Engineer

Senior Validation Engineer

TekWissen LLC

Portsmouth, NH • On-site

$35 - $45/hr

Contractor

Posted 22 days ago

Job description

Overview:  

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  

Job Title:       Senior Validation Engineer
Location:       Portsmouth, NH - 03801
Duration:       7 Months
Job Type:       Temporary Assignment     
Work Type:   Hybrid

Summary
 
The CSV Engineer will act as an individual contributor responsible for ensuring compliance of computerized systems with regulatory requirements and industry standards. The role focuses on implementing best practices, supporting site and process improvement projects, and maintaining GMP-compliant validation and quality systems within a regulated Biotech/Pharma environment.

Responsibilities

  • Act as CSV owner for significant site and process improvement projects, ensuring regulatory compliance and operational efficiency
  • Identify and implement industry best practices using regulatory knowledge and industry networking
  • Collaborate with senior CSV team members during project scoping to identify risks, roadblocks, and efficiency opportunities
  • Perform risk assessments on computerized systems
  • Review and approve change requests, validation test scripts, and protocols
  • Draft, initiate, and review GMP documentation and revisions
  • Execute all aspects of QMS processes including:
  • Change Control (especially related to DCS – DeltaV and MES – Syncade), Deviations, and CAPAs
  • Support validation activities for equipment and computerized systems
  • Perform additional duties as assigned
Required Skills
  • Experience with DeltaV,  Syncade MES
  • Exposure to site-level or large-scale process improvement initiatives
  • Hands-on experience with Distributed Control Systems (DCS) and Manufacturing Execution Systems (MES)
  • Experience performing Change Control, Deviations, and CAPAs in a GMP environment
  • Prior experience leading or supporting projects in Biotech, Pharma, or Biologics industries
  • Strong experience in equipment and/or computerized system validation (CSV)
  • Working knowledge of Controls Automation and Process Control Systems
  • Strong cross-functional collaboration skills
  • Strong attention to detail with the ability to work independently and meet deadlines
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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