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Full Time Trackwise Jobs (NOW HIRING)

Associate Compliance

Billerica, MA ยท On-site

  • Medical

  • Retirement

Full-time Onsite Contract Pay Rate: DoE Job Summary The Temporary - Associate Compliance provides ... Document the evaluation and investigation of Product Quality Complaints within the Trackwise system.

Area Specialist I

Spokane, WA ยท On-site

$41/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Trackwise * MasterControl * ComplianceWire * Annual high performance of 3+ rating or greater ... This is an on-site, full-time position located in Spokane, WA. Hiring Wage: * Area Specialist I: 38 ...

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

Project Manager

Bothell, WA ยท On-site

$94K - $129K/yr

Familiarity with TrackWise. Formalities Location: Bothell, WA Schedule: Full-time Compensation: $94,000 - $129,250 Who We Are AGC Biologics is a global Contract Development and Manufacturing ...

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Showing results 1-20

Full Time Trackwise information

See salary details

$4.9K

$8.7K

$13.4K

How much do full time trackwise jobs pay per month?

As of Aug 13, 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?

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?

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:
Infographic showing various Full Time Trackwise job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 1% Temporary, 13% Contract, and 1% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $104,783 per year, or $50.4 per hour.

Associate Compliance

ProStaff Solutions Inc

Billerica, MA โ€ข On-site

Full-time

Medical, Retirement

Posted 14 days ago


Job description

Our client, a leading pharmaceutical manufacturer, is seeking a detail-oriented Associate Compliance professional to join its Quality Assurance team in Billerica, MA. This is an excellent opportunity for an experienced quality professional to contribute to product quality and patient safety by supporting the evaluation and investigation of product quality complaints in a highly regulated manufacturing environment.
If you're passionate about quality, compliance, and continuous improvement in the life sciences industry, this is an excellent opportunity to make a meaningful impact while advancing your career in pharmaceutical quality assurance.
Full-time Onsite
Contract
Pay Rate: DoE

Job Summary
The Temporary - Associate Compliance provides support in the evaluation and investigation of product quality complaints.
Ensures compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and Quality Management System Standard Operating Procedures related to product complaint handling.
Area of Responsibility
  • Support and assist the QA Complaint Coordinator and the QA Compliance Head on the evaluation and investigation of product quality complaints.
  • Work directly on technical investigations relating to Product Quality Complaints.
  • Document the evaluation and investigation of Product Quality Complaints within the Trackwise system.
  • Other duties as assigned

Qualifications:
  • BS in a scientific field a plus
  • Minimum 3 years related experience in a pharmaceutical/medical device manufacturing regulated environment
  • Working knowledge of cGMPs (current Good Manufacturing Practices) and GDP’s (Good Documentation Practices)
  • Strong working knowledge of MS Word software
  • Must have exceptional writing skills to document the evaluation and investigation processes completed.
  • Experience evaluating and investigating drug/device product complaints a plus
  • Experience using the Trackwise complaint module a plus
  • Superior internal customer service/people skills
  • Ability to manage multiple responsibilities in a fast-paced environment, while performing in an efficient manner

About ProStaff Workforce Solutions
We are a fast growing and successful agency that treats all its clients and candidates with a personal touch. ProStaff Workforce Solutions is a group of industry experts—many hailing from larger agencies—who know their business well and enjoy working in a more hands-on and flexible environment, with attention to detail. Our mission is to match quality people with quality jobs and quality companies to maximize productivity and profitability. We develop long-term relationships and provide a level of customer service and expertise that instill confidence and trust in our client companies and candidates.
Our Values
• Integrity
• Commitment
• Quality
• Diversity
Benefits for eligible employees
• Direct deposit
• Weekly pay
• Medical benefits
• 401(k) Plan
Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.
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