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Experience With Valgenesis Jobs (NOW HIRING)

Intellectt Inc

Validation Engineer (CQV)

Devens, MA

Experience working in large-scale cell culture environments . * Familiarity with steam systems, SIP/CIP processes, and flow path verification. * Experience executing protocols in ValGenesis or ...

Avispa Technology

MES Validation Engineer

Hillsboro, OR · On-site +1

$70 - $80/hr

Experience with regulated life sciences platforms, including ERP systems, ValGenesis, LIMS, SCADA, or similar technologies. * Experience with MES Pharma Suite Writing is preferred. * Professional ...

ACL Digital

GxP System admininstrator

San Mateo, CA · Hybrid

... Hands-on experience with validation and quality systems (ValGenesis or equivalent, Veeva QMS) Proficiency with project and reporting tools, including Azure DevOps, JIRA, MS Visio Nice to Have ...

Avispa Technology

MES Validation Engineer

Hillsboro, OR · Remote

$70 - $80/hr

Experience with regulated life sciences platforms, including ERP systems, ValGenesis, LIMS, SCADA, or similar technologies. * Experience with MES Pharma Suite Writing is preferred. * Professional ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

Experience with DeltaV, Rockwell, Kneat, or ValGenesis. * Biologics or sterile manufacturing experience. * Bachelor's degree in Engineering or related field. Thanks & Regards, Vyshnavi Recruiter ...

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Experience With Valgenesis information

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How much do experience with valgenesis jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for experience with valgenesis in the United States is $17.79, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $17.79 per hour, depending on experience, location, and employer.

What is the difference between Experience With Valgenesis vs Clinical Data Coordinator?

AspectExperience With ValgenesisClinical Data Coordinator
Required CredentialsKnowledge of clinical data management systems, certifications in clinical researchTypically requires a degree in health sciences or related field, certifications in clinical data management
Work EnvironmentPharmaceutical or biotech companies, clinical research organizationsHospitals, research institutions, clinical trial sites
Industry UsageUsed in clinical data management, electronic data capture systemsManaging clinical trial data, ensuring data accuracy and compliance

Experience With Valgenesis involves working with electronic data capture systems in clinical research, focusing on data management and system proficiency. Clinical Data Coordinators handle clinical trial data collection and validation. Both roles require familiarity with clinical data processes, but Experience With Valgenesis emphasizes system-specific skills, while Clinical Data Coordinators focus on data integrity and compliance in clinical settings.

What is the ValGenesis?

ValGenesis is a digital validation platform used in regulated industries to manage and automate validation processes for manufacturing and quality systems. It helps ensure compliance with industry standards such as FDA and ISO by providing electronic documentation and audit trails. Professionals working with ValGenesis often need knowledge of validation protocols, regulatory requirements, and software implementation.

What is experience with ValGenesis and why is it important?

Experience with ValGenesis refers to familiarity and proficiency in using the ValGenesis platform, which is a digital validation lifecycle management system widely used in regulated industries like pharmaceuticals and biotechnology. Professionals with ValGenesis experience are adept at managing validation documents, automating workflows, and ensuring compliance with regulatory standards such as FDA and EMA requirements. This expertise is important because it helps organizations streamline validation processes, reduce errors, and maintain comprehensive audit trails, ultimately supporting product quality and regulatory compliance.

How does experience with ValGenesis impact collaboration within a quality assurance or validation team?

Having experience with ValGenesis significantly enhances collaboration within quality assurance and validation teams by streamlining documentation, approvals, and compliance workflows. As ValGenesis is an electronic validation lifecycle management system, familiarity with its platform enables team members to efficiently manage validation documents, track changes, and communicate updates in real-time. This reduces bottlenecks and improves transparency, allowing cross-functional teams—such as quality, IT, and manufacturing—to work together more effectively and maintain regulatory compliance. Employers often value candidates who can leverage ValGenesis to foster a more integrated and agile validation process.

Is ValGenesis a good company to work for?

ValGenesis is a company specializing in digital validation solutions, often hiring for roles related to software development, project management, and quality assurance. Employee reviews indicate a focus on innovation and a collaborative environment, but experiences can vary based on role and location.

What key skills and qualifications are needed to succeed in a role requiring experience with ValGenesis, and why are they important?

To excel in a position requiring experience with ValGenesis, you need a background in life sciences or engineering and a solid understanding of validation lifecycle management processes. Familiarity with the ValGenesis Validation Lifecycle Management System (VLMS), electronic documentation, and regulatory compliance standards such as FDA 21 CFR Part 11 is typically expected. Attention to detail, strong analytical thinking, and effective communication skills help individuals stand out in this role. These competencies are vital to ensure accurate, compliant, and efficient validation processes in regulated environments like pharmaceuticals or biotech.

What is the interview process for ValGenesis?

The interview process for a role involving ValGenesis typically includes an initial phone or video screening, followed by technical or skills assessments related to the company's software and quality management systems. Candidates may also participate in in-person interviews with team members and be evaluated on their understanding of validation processes and relevant tools.

What type of company is ValGenesis?

ValGenesis is a technology company that provides digital validation solutions for the life sciences and manufacturing industries. It specializes in cloud-based software to streamline validation processes, ensuring compliance with industry regulations. Employees in related roles often work with validation protocols, quality systems, and regulatory standards.
Infographic showing various Experience With Valgenesis job openings in the United States as of June 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $37,000 per year, or $17.8 per hour.
MES Validation Engineer

MES Validation Engineer

Dawar Consulting, Inc.

Hillsboro, OR • Remote

$75 - $84/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 3 days ago

Job description

This is a remote position.

Our client, a world leader in the life sciences and diagnostics industry, is looking for a “MES Validation Engineer” in
Hillsboro, OR

Job Duration: Long Term Contract (Possibility Of Extension)
Pay Rate: $75/hr - $84/hr on W2 DOE
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

We are seeking an experienced MES Validation Engineer to support the deployment and validation of Manufacturing Execution Systems (MES) within a GMP-regulated biotechnology manufacturing environment. The successful candidate will be responsible for developing and executing validation strategies, protocols, and test scripts for computerized systems while ensuring compliance with FDA, EMA, GxP, and industry standards.

Key Responsibilities
  • Develop, author, review, and execute validation protocols, test scripts, and validation reports for MES and computerized systems.
  • Support implementation and validation of Rockwell FactoryTalk PharmaSuite and related manufacturing systems.
  • Collaborate with IT/OT, Quality Assurance, Manufacturing, System Owners, and Business Process Owners to ensure validation activities align with GMP requirements.
  • Develop validation strategies, risk assessments, traceability matrices, and testing plans.
  • Execute Computer System Validation (CSV) activities including IQ, OQ, PQ, UAT, and system qualification.
  • Ensure compliance with FDA, EMA, 21 CFR Part 11, GAMP 5, and Data Integrity requirements.
  • Support change controls, deviations, CAPA investigations, and audit readiness activities.
  • Manage testing execution, defect tracking, and validation deliverables throughout the project lifecycle.
  • Work with regulated systems such as MES, LIMS, SCADA, ERP, and electronic records systems.
  • Provide technical guidance on validation best practices and system compliance.
Required Qualifications
  • Bachelor's degree in Biomedical Engineering, Computer Science, Biology, Biochemistry, Chemistry, Biotechnology, Regulatory Affairs, Information Technology, or related Life Sciences field.
  • Minimum 5 years of experience in Computer System Validation (CSV) or Validation Engineering within a GMP-regulated environment.
  • Experience with Rockwell FactoryTalk PharmaSuite.
  • Strong knowledge of FDA, EMA, GxP, GAMP 5, and 21 CFR Part 11 requirements.
  • Experience authoring and executing validation protocols and test scripts.
  • Experience with risk assessments, change control, deviations, and CAPA processes.
  • Strong verbal and written communication skills.
  • Ability to work effectively in cross-functional teams.
Preferred Qualifications
  • Experience with ValGenesis, LIMS, SCADA, ERP systems, DeltaV, or other regulated manufacturing platforms.
  • Professional certifications such as CQE, CSQE, or CSVS.
  • Experience supporting MES implementation projects.
  • Knowledge of pharmaceutical, biotech, cell therapy, gene therapy, or biologics manufacturing operations.
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

If interested, please send your updated resume to hr@dawarconsulting.com/kavitha@dawarconsulting.com