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Full Time Trackwise Jobs (NOW HIRING)

Lonza

Senior Quality Program Specialist

Walkersville, MD

$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 ...

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 ...

Inteldot

Document Coordinator

Barceloneta, PR · On-site

Employment type: Full time and onsite role Position Overview We are seeking an experienced ... Experience with document management systems such as Veeva, TrackWise, MasterControl, or similar ...

Home | NIRA

QMS Administrator/Developer

Hyattsville, MD · On-site

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 ...

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 ...

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All JobsFull Time Trackwise Jobs

Full Time Trackwise information

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$4.9K

$8.7K

$13.4K

How much do full time trackwise jobs pay per month?

As of Jun 30, 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.
More about Full Time Trackwise jobs
What cities are hiring for Full Time Trackwise jobs? Cities with the most Full Time Trackwise job openings:
What are the most commonly searched types of Trackwise jobs? The most popular types of Trackwise jobs are:
What job categories do people searching Full Time Trackwise jobs look for? The top searched job categories for Full Time Trackwise jobs are:
Full Time Trackwise jobs near you
Infographic showing various Full Time Trackwise job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $104,783 per year, or $50.4 per hour.

Microbiology Sterilization I

CIS International LLC

Salinas, PR

Full-time

Posted 15 days ago

Job description

Main Responsibilities:
  • Support EO sterilization and microbiological testing activities within a regulated manufacturing environment.
  • Perform microbiological analyses on raw materials, in-process materials, release samples, and stability samples.
  • Prepare, clean, disinfect, sterilize, store, and handle laboratory instruments, materials, products, and supplies.
  • Support sterilization validations including protocol execution, documentation, and report preparation.
  • Interpret and evaluate analytical results against established specifications and support corrective action activities when necessary.
  • Assist in developing, validating, and implementing controlled environment methods and laboratory procedures.
  • Perform qualitative and quantitative testing using standard laboratory equipment and automated instrumentation.
  • Support methodology transfer activities from R&D into manufacturing or laboratory operations.
  • Maintain accurate technical documentation, validation records, protocols, and reports in compliance with GDP requirements.
  • Collaborate with Manufacturing, Quality, Engineering, Regulatory, and R&D teams to support sterilization and microbiological initiatives.
  • Participate in continuous improvement activities related to sterilization, laboratory operations, and microbiological processes.
  • Follow FDA regulations, ISO standards, and company quality procedures.
*Other duties may be assigned.*RequirementsEducation
  • Minimum 3 year of relevant experience in the regulated industry.
  • Bachelor’s degree in Science (Microbiology, Biology, Biotechnology, Biomedical Sciences).
  • Entry-level candidates are acceptable.
Required Skills & Qualifications
  • Knowledge of EO sterilization processes.
  • Familiarity with FDA regulations, ISO 11135, ISO 11737, and related sterilization and microbiological standards.
  • Strong technical documentation and report-writing skills.
  • Ability to support sterilization validations, protocols, and testing activities.
  • Strong analytical and problem-solving skills.
  • Ability to communicate findings clearly and collaborate effectively with cross-functional teams including Manufacturing, Quality, Regulatory, and R&D.
  • Fully bilingual (English and Spanish).
Preferred Qualifications
  • Experience in regulated manufacturing, pharmaceutical, biotechnology, or medical device industries.
  • Experience with TrackWise or similar quality management systems.
  • Knowledge of environmental monitoring and controlled environments.
  • Exposure to validation and laboratory quality systems.
Technical Skills
  • Microsoft Office Suite
  • TrackWise
  • Agile environment exposure
  • Technical documentation
  • Sterilization validation support
  • Microbiological testing techniques
  • Controlled environment practices
Work Methodology:
  • 100% on site job
  • Full time job
  • 1 year of first contract term with expectation of continuity based on performance and budget
  • Location: Salinas, PR
  • Administrative shift
  • Type of industry: Medical devices