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Full Time Trackwise Jobs (NOW HIRING)

WuXi Biologics

Scientist I, Quality Control

Cranbury, NJ · On-site

$60K - $95K/yr

Qualifications * Full-time undergraduate degree or above, majoring in biology, chemical engineering ... TrackWise, Master Control, LIMS). Ability to adapt between strategic and tactical thinking/planning ...

Gifthealth

QA Specialist - Pharmacy Operations

Mesa, AZ · On-site

$60K - $75K/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 ...

CIS International LLC

PR

$101K - $131K/yr

Knowledge in SAP, Trackwise, electronic batch records (PAS/X) , and documents management systems ... Full on site job in Juncos, PR * Full time job * Expected project duration: 6 months for the first ...

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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.
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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.

Scientist I, Quality Control

WuXi Biologics

Cranbury, NJ • On-site

$60K - $95K/yr

Full-time

Posted 19 days ago

Key responsibilities

  • Perform raw material and compendial testing and sampling, including tests such as FTIR, pH, color, clarity, visible and subvisible particles, and osmolarity.

  • Record and organize experimental data in accordance with Good Document Management Practices to ensure data integrity.

  • Manage raw material samples, sampling rooms, and sample storage areas to ensure proper sampling processes and storage control.

Job description

Job Title - Scientist l, Quality Control - RM/Compendial Testiing and Sampling
Work Location - Cranbury NJ
Job Summary
The QC RM/Compendial Scientist is responsible for the quality and on-time completion of raw material/compendial testing and sampling. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates good oral and written communication skills and actively contributes to timely training, report generation and good GMP documentation and archival.
Job Responsibilities
  • Understand GMP and follow instructions on the documents.
  • Perform raw material/compendial testing including but not limit to FTIR, pH, Color, Clarity, visible and subvisible particles, osmolarity, etc.
  • Able to support Raw Material sample sampling and its transporting needs in/between the various building sites in Cranbury or other US sites (when needed).
  • Management of raw material samples, raw material sampling room, sample storage room and regulatory retain sample room, etc., and ensuring the sampling process and storage of raw material samples are conducted properly and within control.
  • Support reagents/consumables inventory management to ensure consistent QC RM/Compendial operation needs.
  • Record and organize experimental data in accordance with "Good Document Management Practices" to ensure data integrity.
  • Ensure compliance to training, preparation, documentation and general lab maintenance requirements for Industry Standards and/or Regulations.
  • Assist in preparing or executing validation documents to support new materials, process changes and qualifications.
  • Maintains laboratory notebooks and worksheets for QC tasks as required.
  • Able to work at weekend when needed.
  • Support shift work when needed.
  • Any other duties assigned by the supervisor (when applicable).

Qualifications
  • Full-time undergraduate degree or above, majoring in biology, chemical engineering, chemistry, pharmacy or related majors.
  • Bachelor's degree: 6+ years of experience in the professional field
  • Master's degree: 4+ years of experience in the professional field
  • PhD: no requirement
  • Candidate must possess willingness to learn analytical and QC operations of pharmaceutical industry, understand current regulations and industry trends of biologics product development, characterization and manufacturing testing requirement including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance.
  • Basic familiarity with analytical instruments and methodologies, such as pH, turbidity meter, HIAC, etc, is preferred.
  • Basic experience with software and information systems (eg. TrackWise, Master Control, LIMS). Ability to adapt between strategic and tactical thinking/planning and manage multiple priorities to achieve department and site objectives.
  • Ability to understand technical data
  • Experience in planning and ability to solve QC technical and operation problems.
  • Be able to raise issues immediately to supervisor and work with supervisor when in doubt.
  • Proficiency in English is required. Good communications skills (verbal, written, and presentation skills).
  • Effectively exchange information or discuss clearly framed issues or ideas with colleagues.

The anticipated pay range for this position is $60,000 - $95,000
The 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.

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