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Trackwise Consultant Jobs (NOW HIRING)

CYNET SYSTEMS

Quality Control Analyst I

Swiftwater, PA · On-site

$27 - $32/hr

Support SAP, TrackWise, and LIMS system activities. * Participate in team meetings, safety meetings ... S. states and Canada, we support thousands of consultants through our expansive, high-performing ...

ASK Consulting

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Logistics Associate (277398)

Portsmouth, NH · On-site

$22 - $24/hr

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be ... Utilizes DMS and Trackwise for assigned area. * Perform other duties as they are assigned to ...

DivIHN Integration Inc

CAPA/NCR Writer

Round Lake, IL · On-site

... Consultation and facilitation skills. 6. Understanding of statistics in support of fact based ... Hands-on experience with TrackWise or a similar quality management system 15. Experience conducting ...

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Trackwise Consultant information

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How much do trackwise consultant jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for trackwise consultant in the United States is $52.81, according to ZipRecruiter salary data. Most workers in this role earn between $31.25 and $70.91 per hour, depending on experience, location, and employer.

What is the difference between Trackwise Consultant vs Trackwise Developer?

AspectTrackwise ConsultantTrackwise Developer
CredentialsTypically requires a background in pharmaceutical or regulatory industries, with knowledge of Trackwise software and certifications in quality management systemsOften has technical skills in software development, programming, and Trackwise customization, with relevant IT or QA certifications
Work EnvironmentWorks with clients to implement, optimize, and support Trackwise solutions in regulated industriesFocuses on developing, customizing, and maintaining Trackwise applications and modules
Employer & Industry UsageCommonly employed by pharmaceutical, biotech, and life sciences companies for quality and compliance managementTypically employed by software vendors or internal IT teams within regulated industries

In summary, a Trackwise Consultant primarily advises and supports clients in implementing and optimizing Trackwise systems, while a Trackwise Developer focuses on the technical development and customization of the software itself. Both roles require specific industry knowledge but differ in their core responsibilities and skill sets.

What types of projects do Trackwise Consultants typically work on, and how do they collaborate with quality and IT teams?

Trackwise Consultants are often engaged in projects focused on implementing, configuring, or upgrading the TrackWise Quality Management System for organizations in regulated industries, such as pharmaceuticals and biotechnology. They regularly work with cross-functional teams, including quality assurance, IT, and business stakeholders, to gather requirements, design workflows, and ensure compliance with industry standards. Collaboration involves frequent meetings, documentation reviews, and user training sessions to align system capabilities with business processes and regulatory needs. This role offers opportunities to develop expertise in quality systems and build strong project management skills.

What are the key skills and qualifications needed to thrive as a Trackwise Consultant, and why are they important?

To excel as a Trackwise Consultant, you need expertise in quality management systems, regulatory compliance, and a strong understanding of the Trackwise platform, often supported by a degree in computer science, engineering, or life sciences. Familiarity with technical tools such as Trackwise configuration, workflow customization, SQL databases, and experience with GxP compliance are typically required. Outstanding problem-solving, communication, and project management skills help consultants effectively gather requirements and deliver tailored solutions to clients. These competencies are vital to ensure organizations maintain regulatory standards and optimize their quality processes using Trackwise.

What is a Trackwise Consultant?

A Trackwise Consultant is a professional who specializes in the implementation, customization, and support of Trackwise, which is a quality management software developed by Sparta Systems. These consultants work with organizations—often in regulated industries like pharmaceuticals or life sciences—to streamline and automate their quality and compliance processes using Trackwise. Their responsibilities may include gathering requirements, configuring the software, training users, and ensuring that the system meets regulatory standards. They play a critical role in helping companies maintain compliance and improve operational efficiency.
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What are the most commonly searched types of Trackwise Consultant jobs? The most popular types of Trackwise Consultant jobs are:
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Trackwise Consultant jobs near you
Infographic showing various Trackwise Consultant job openings in the United States as of May 2026, with employment types broken down into 3% Locum Tenens, and 97% Full Time. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $109,849 per year, or $52.8 per hour.

Jr. Validation Specialist

Mirus Consulting Group

Humacao, PR • On-site

Full-time

Posted 18 days ago

Job description

mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved.
Position Summary
The Jr Validation Specialist supports validation lifecycle activities related to manufacturing processes, equipment, utilities, software systems, and process improvements. This role is responsible for protocol generation, execution, discrepancy resolution, and validation documentation while ensuring compliance with internal procedures, FDA regulations, and medical device quality standards. The position provides excellent exposure for professionals seeking to expand their validation expertise within a world-class medical device manufacturing environment.
Key Responsibilities
  • Support full validation lifecycle activities, including planning, execution, and closure of validation efforts.
  • Generate, execute, review, and maintain validation protocols and reports (IQ/OQ/PQ).
  • Support commissioning and qualification activities for manufacturing equipment, systems, and processes.
  • Perform validation assessments, discrepancy investigations, and manage protocol deviations.
  • Collaborate with cross-functional teams, including Engineering, Manufacturing, Quality, Automation, and Operations.
  • Ensure all documentation complies with Good Documentation Practices (GDP), cGMP, FDA regulations, ISO 13485, and internal quality system requirements.
  • Support risk assessments and implementation of corrective and preventive actions (CAPA), as required.
  • Participate in troubleshooting activities associated with validation execution and equipment or process performance issues.
  • Support change control activities, including validation impact assessments and documentation updates.
  • Utilize systems such as SAP and TrackWise to support documentation, investigations, and workflow processes.
  • Contribute to continuous improvement initiatives and support execution readiness for ongoing and new projects.
Minimum Qualifications
  • Bachelor's Degree in: Engineering, Life Sciences, Chemistry, Biotechnology or a related technical field.
  • 1-3 years of experience in one or more of the following areas:
    • Validation
    • Quality
    • Engineering
    • Manufacturing support
  • Experience within Medical Device, Pharmaceutical, or other regulated industries.
Preferred Qualifications
  • Experience generating and executing IQ/OQ/PQ validation protocols.
  • Working knowledge of: cGMP, GDP, FDA regulations, ISO 13485.
  • Familiarity with systems such as: TrackWise, SAP.
  • Experience with validation documentation and technical writing.
  • Strong troubleshooting, analytical, and problem-solving skills.
  • Bilingual (English/Spanish) preferred.
This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.

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