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Full Time Trackwise Jobs (NOW HIRING)

Lonza

Senior Quality Program Specialist

Walkersville, MD · On-site

$95K - $153K/yr

The full-time base annual salary for this position is expected to range between $95,000 to $153,000 ... Perform quality system activities within DMS, LIMS, and TrackWise (Change Control, CAPA, Deviations ...

Eurofins

Analytical Chemist

Indianapolis, IN · On-site

UV * Smart Lab and Trackwise software experience a plus Qualifications * Strong computer ... The position is full-time, Monday through Friday, 8am-5 pm. Must have ability to work overtime as ...

Innovative Career Resources & Staffing

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Complaint Specialist

Irvine, CA · On-site

$70K - $75K/yr

... a Full Time, Direct Hire basis. The Complaints Specialist will ensure appropriate product ... Experience in TrackWise or similar electronic systems. * Basic knowledge of GMPs, ISO 13485, and ...

Cosette Pharmaceuticals Inc.

Good working knowledge of PCs and Microsoft applications, QAD, and Trackwise system. Work ... Employment Type: Full Time

NIRA, Inc.

QMS Administrator/Developer

Hyattsville, MD · On-site

$100K/yr

This is a full-time, hybrid position. Candidates should expect to work in-person three plus days a ... TrackWise, SharePoint, or similar platforms. * Familiarity with regulated environments such as life ...

NIRA, Inc.

QMS Administrator/Developer

Hyattsville, MD · On-site

$100K/yr

This is a full-time, hybrid position. Candidates should expect to work in-person three plus days a ... TrackWise, SharePoint, or similar platforms. * Familiarity with regulated environments such as life ...

Gifthealth

QA Specialist - Virtual Hub

$63K - $74K/yr

Experience with a QMS/eQMS (e.g., TrackWise or similar) including change control, document control ... Schedule : Full-time * May require additional availability or flexibility for audits or ...

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Full Time Trackwise information

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$13.4K

How much do full time trackwise jobs pay per month?

As of Jul 22, 2026, the average monthly pay for full time trackwise in the United States is $8,731.92, according to ZipRecruiter salary data. Most workers in this role earn between $5,208.33 and $12,250.00 per month, depending on experience, location, and employer.

What are the typical challenges a Full Time Trackwise professional may encounter when managing quality management system (QMS) workflows?

Full Time Trackwise professionals frequently face challenges such as ensuring data integrity across multiple QMS processes, adapting to evolving regulatory requirements, and facilitating smooth collaboration between cross-functional teams. Managing complex workflows and troubleshooting system issues can require strong problem-solving skills and attention to detail. Additionally, professionals need to stay current with Trackwise updates to maximize system efficiency and maintain compliance within the organization.

What is a Full Time Trackwise specialist?

A Full Time Trackwise specialist is a professional who manages and maintains the Trackwise quality management software, commonly used in regulated industries like pharmaceuticals and biotechnology. Their responsibilities include configuring the system, troubleshooting issues, training users, and ensuring compliance with quality standards. They often work with cross-functional teams to streamline processes such as document control, audits, and corrective actions. This role typically requires strong technical skills, attention to detail, and an understanding of industry regulations.

What is the difference between Full Time Trackwise vs Full Time Quality Assurance Specialist?

AspectFull Time TrackwiseFull Time Quality Assurance Specialist
Required CredentialsDegree in Life Sciences, GMP trainingDegree in Life Sciences, GMP/ISO certifications
Work EnvironmentPharmaceutical manufacturing, quality control labsPharmaceutical, biotech, or manufacturing settings
Employer & Industry UsageUsed in pharmaceutical and biotech industries for software validationCommonly employed in quality assurance roles across similar industries

Full Time Trackwise roles focus on software validation and compliance within pharmaceutical manufacturing, often requiring GMP knowledge. Full Time Quality Assurance Specialists oversee overall quality processes, including audits and documentation. While both roles emphasize quality and compliance, Trackwise positions are more specialized in validation software, whereas QA Specialists have broader quality responsibilities.

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

To thrive as a TrackWise Administrator, you need a solid understanding of quality management processes, database management, and a background in life sciences or regulated industries. Familiarity with TrackWise software, SQL, and relevant certifications like TrackWise Administrator Certification are typically required. Attention to detail, problem-solving abilities, and strong communication skills help ensure system integrity and effective user support. These competencies are crucial for maintaining compliance, optimizing workflows, and supporting quality assurance initiatives.
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Full Time Trackwise jobs near you
Infographic showing various Full Time Trackwise job openings in the United States as of July 2026, with employment types broken down into 74% Full Time, 24% Part Time, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $104,783 per year, or $50.4 per hour.
Sr. Quality Application Specialist (Science)/ Sr. Quality Engineer (Engineer)

Sr. Quality Application Specialist (Science)/ Sr. Quality Engineer (Engineer)

CIS International LLC

Juncos, PR

$86K - $116K/yr

Full-time

Re-posted 19 days ago

Job description

Key Requirements:

  • Bachelor's degree in Engineering or Science.
  • Knowledge and experience with IT systems and integrations with manufacturing equipment.
  • Minimum of 4 years of experience in Quality Systems, Computer System Validation (CSV), or regulated IT environments.
  • Strong expertise in CSV lifecycle management.
  • Experience authoring and reviewing validation documentation, including Validation Plans, Risk Assessments, IQ/OQ/PQ protocols, reports, and SOPs.
  • Knowledge of FDA, GxP, ISO, and data integrity requirements.
  • Experience managing documentation changes and change control processes.
  • Strong quality and compliance leadership skills.
  • Excellent cross-functional communication and stakeholder management abilities.

Preferred Qualifications:

  • Experience with electronic Quality Management Systems (QMS) such as Trackwise, ETQ, Master Control, or Veeva.
  • Experience supporting regulatory audits and inspections related to computerized systems.

Work Methodology:

  • 100% on site job
  • Full time job
  • Location: Juncos, PR
  • Administrative shift
  • Type of industry: Medical devices
  • Expected hiring month: July 2026
  • Timeframe: November 2026