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Freelance Pharmaceutical Validation Jobs (NOW HIRING)

Jobgether

... of pharmaceutical manufacturing processes, GMP requirements, Computerized System Validation (CSV ... Freelance contract arrangement with flexible remote collaboration. * Full-time engagement of ...

Solomon Page

Raw Materials Specialist

Kenilworth, NJ · On-site

$35/hr

Create, revise, and validate internal raw material specifications and test methods, ensuring ... food, or pharmaceuticals. * Requires proficiency in Microsoft Office and prefers candidates ...

ProPharma Group

... device, and pharmaceutical organizations of all sizes to confidently advance scientific ... Lead and support SEC-HPMC method development and validation for Phase 3 registration activities

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Freelance Pharmaceutical Validation information

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$15

$26

$45

How much do freelance pharmaceutical validation jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for freelance pharmaceutical validation in the United States is $26.09, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $30.53 per hour, depending on experience, location, and employer.

What is the difference between Freelance Pharmaceutical Validation vs Pharmaceutical Validation Specialist?

AspectFreelance Pharmaceutical ValidationPharmaceutical Validation Specialist
CredentialsRelevant certifications, industry experienceSame as freelance, often with additional company-specific training
Work EnvironmentContract-based, remote or on-site, multiple clientsFull-time, on-site or office-based within a company
Employer & Industry UsageUsed by independent contractors serving pharmaceutical companiesEmployed directly by pharmaceutical firms or contract organizations

Freelance Pharmaceutical Validation professionals work independently, often on multiple projects, offering flexibility. In contrast, Pharmaceutical Validation Specialists are typically employed full-time within a company, focusing on ongoing validation processes. Both roles require similar certifications and industry knowledge, but their work settings and employment structures differ significantly.

What cities are hiring for Freelance Pharmaceutical Validation jobs? Cities with the most Freelance Pharmaceutical Validation job openings:
What are the most commonly searched types of Pharmaceutical Validation jobs? The most popular types of Pharmaceutical Validation jobs are:
What states have the most Freelance Pharmaceutical Validation jobs? States with the most job openings for Freelance Pharmaceutical Validation jobs include:
What job categories do people searching Freelance Pharmaceutical Validation jobs look for? The top searched job categories for Freelance Pharmaceutical Validation jobs are:
Freelance Pharmaceutical Validation jobs near you
Infographic showing various Freelance Pharmaceutical Validation job openings in the United States as of July 2026, with employment types broken down into 58% Full Time, 12% Part Time, 2% Temporary, 22% Contract, and 6% Nights. Highlights an 60% Physical, 2% Hybrid, and 38% Remote job distribution, with an average salary of $54,267 per year, or $26.1 per hour.

Senior Werum PAS-X MES L2 Support & Integration Specialist

Jobgether

Remote

Contractor

Posted 6 days ago

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Werum PAS-X MES L2 Support & Integration Specialist based in Netherlands.

As a Senior Werum PAS-X MES L2 Support & Integration Specialist, you will play a critical role in maintaining reliable manufacturing operations within a global pharmaceutical environment. You will provide expert-level support for Manufacturing Execution Systems, troubleshoot complex production issues, and ensure seamless integration between MES and enterprise platforms. Working closely with manufacturing, quality, validation, and IT teams, you will help maintain compliant, efficient, and continuously improving digital manufacturing processes. This remote freelance opportunity is ideal for an experienced MES professional who enjoys solving technical challenges, improving operational stability, and contributing to mission-critical pharmaceutical production systems.

Accountabilities
  • Provide Level 2 application support for Werum PAS-X MES across manufacturing and packaging operations, ensuring system availability and operational continuity.
  • Monitor, investigate, troubleshoot, and resolve MES incidents, execution failures, and integration issues according to agreed service levels.
  • Perform root cause analysis for recurring technical problems and coordinate resolution efforts with internal teams, vendors, and advanced support teams.
  • Manage Werum PAS-X administration activities, including user management, security roles, permissions, and system configuration.
  • Support the full lifecycle of Master Batch Records (MBR) and Electronic Batch Records (EBR), including updates, deployments, maintenance, and troubleshooting.
  • Maintain and improve integrations between Werum PAS-X and enterprise systems, particularly SAP PP-PI, ensuring reliable data exchange and interface performance.
  • Collaborate with Manufacturing, Quality Assurance, Validation, and IT stakeholders to support compliant MES operations.
  • Participate in validation activities, change management processes, system releases, enhancements, and continuous improvement initiatives.
  • Create and maintain technical documentation, standard operating procedures, knowledge articles, and operational guidelines.
  • Provide production support during critical manufacturing activities and ensure timely resolution of business-impacting issues.
Requirements
  • Minimum 5 years of experience supporting Werum PAS-X MES within pharmaceutical, biotechnology, life sciences, or GMP-regulated manufacturing environments.
  • Strong hands-on experience providing Level 2 support for Manufacturing Execution Systems in production environments.
  • Proven expertise in Werum PAS-X administration, configuration, and operational support.
  • Experience managing Master Batch Records (MBR) and Electronic Batch Records (EBR) throughout their lifecycle.
  • Mandatory experience with MES integrations, particularly SAP PP-PI connectivity and troubleshooting.
  • Strong understanding of pharmaceutical manufacturing processes, GMP requirements, Computerized System Validation (CSV), and regulated environments.
  • Experience with incident management, root cause analysis, change control, and production issue resolution.
  • Excellent analytical and problem-solving skills with the ability to manage complex technical challenges.
  • Knowledge of manufacturing automation environments, ISA-95 architecture, middleware technologies, SCADA, PLCs, historian platforms, or Industry 4.0 solutions is a plus.
  • Familiarity with ITIL practices or certification is considered an advantage.
  • Strong communication skills and the ability to collaborate effectively with technical and business stakeholders.
Benefits
  • Fully remote working opportunity within Europe.
  • Freelance contract arrangement with flexible remote collaboration.
  • Full-time engagement of approximately 40 hours per week.
  • Opportunity to work with a global pharmaceutical organization on critical digital manufacturing initiatives.
  • Exposure to advanced MES, enterprise integration, and regulated manufacturing technologies.
  • Opportunity to contribute to impactful projects within the life sciences and pharmaceutical sectors.
  • Start date planned for June/July 2026.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
 Why Apply Through Jobgether? 
 
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
 
 
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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.
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