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Full Time Trackwise Jobs (NOW HIRING)

React Health

Senior, Complaints Manager

Dublin, OH · On-site

$98K - $155K/yr

Senior, Complaints Manager FULL-TIME/PART-TIME : Full time LOCATION: Dublin, OH React Health is a ... TrackWise * Experience and understanding of the overall business environment and required ...

Visium Resources, Inc.

Project Manager

Boulder, CO · On-site

Visium Resources has been asked to identify qualified candidates for a full time position as a ... Familiarity with Kneat, TrackWise, Veeva, or electronic validation systems. * Previous consulting ...

CSL

Batch Release Specialist

Holly Springs, NC · On-site

Quality Assurance Job Type: Full Time Location: Holly Springs, North Carolina, United States ... TrackWise) used in support of Clinical Supply Quality. 2.Oversee and ensure compliance to GMP/GSP ...

Zoetis

Site Quality Control Analyst

Rathdrum, ID · On-site

$22 - $29.50/hr

Empower 3, Trackwise, SAP, Document Management, Learning This position will require fluent use of ... Full time Legal statement as below This job advert indicates the general nature and level of work ...

nVent

Quality Manager II

Anoka, MN

$105K - $195K/yr

Proficiency with enterprise quality systems and tools such as Intelex, TrackWise, CATSWEB, or ... We provide a broad benefits package with meaningful programs for eligible full-time employees that ...

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How much do full time trackwise jobs pay per month?

As of Jun 7, 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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What cities are hiring for Full Time Trackwise jobs? Cities with the most Full Time Trackwise job openings:
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Full Time Trackwise jobs near you
Infographic showing various Full Time Trackwise job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 93% Full Time, and 6% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $104,783 per year, or $50.4 per hour.

Scientist, Quality Control Operation

WuXi Biologics

Cranbury, NJ • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Job Title - Scientist, Quality Control
Work Location - Cranbury, NJ
Job Summary:
The Scientist-QC Operations will be responsible for QC sample management, RS management, and QC stability study program to support QC GMP activities, including but not limited to in-time and properly sample/RS receiving, aliquoting, storage, and distribution for testing, and stability study protocol writing/reviewing/revising, stability sample receiving, aliquoting for stability study initiation, storage, pulling, aliquoting and distribution for testing in time and correctly to ensure on-time delivery of test results, validation data and other QC deliverables to internal and external clients. Also as inventory management QC GMP documentation archive backup to support QC inventory management and QC GMP documentation archive as needed. Strong communication, detail orientation, and time management skills are desired.
Responsibilities:

  • Responsible for QC sample management, including but not limited to receiving, storage, aliquoting, distributing, tracking, and disposing of QC testing sample and reference standards.
  • Responsible for stability sample management, including but not limited to sample receiving, aliquoting, distributing, tracking, and disposing of stability backup sample.
  • Responsible for reference standard (RS) management, including RS receiving, aliquoting, storage, and distribution.
  • Perform technical review of sampling plans, stability study protocols, RS aliquoting, qualification and re-qualification protocols.
  • Perform RS, regulatory retain sample, and stability samples annual inventory checking.
  • Coordinate with QC Functional Leads (QCFL) to ensure timely cleanup, reconciliation, and disposal of project-related stability and RS samples upon project completion.
  • Support QC lab inventory management, including but not limited to QC lab inventory ordering, receiving, storage, distribution, inventory tracking.
  • Ensure compliance with QC operation related documentation and training for company's requirements
  • Request sample/RS and stability management-related control paper forms and logbooks for sample storage refrigerators, freezers and chambers from QA as needed.
  • Responsible for maintenance of all refrigerators/freezers used for sample/RS/stability sample storage well organized and clean and responding to alarms and executing corrective actions to protect sample integrity.
  • Responsible for weekly in-process sample clean up and disposal.
  • Perform all activities in compliance with applicable safety policies, quality systems, and cGMP requirements.
  • Mentor junior QC operation staff and provide technical guidance and support.
  • Perform other duties assigned by management to support overall QC operations.
  • Qualifications:
  • Bachelor's degree: 4+ years of experience in the related professional field. Master's degree and above: 2+ years of experience in the related professional field.
  • Full-time undergraduate degree or above, majoring in biology, chemical engineering, chemistry, pharmacy or related majors.
  • Be skilled at reading, writing, and understanding GMP documentation.
  • Strong attention to detail and organizational skills
  • Good computer operation skills in Microsoft Word, Excel, PowerPoint etc.
  • Broad knowledge and experience in GMP regulations.
  • High awareness of confidentiality and responsibility.
  • Detail oriented and effective time management.
  • Critical thinking, scientific reasoning, planning and problem-solving skills.
  • Experience with a wide variety of software and information systems (e.g. LIMS, TrackWise, MC, etc.).
  • Be able to work independently as well as a good team player.
Salary range for this position is 60,200-96,300 Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

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