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Full Time Trackwise Jobs (NOW HIRING)

Stability Administrator

Bedford, OH · On-site

$44K - $74K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Bedford, Ohio Job Type: Full-Time About Us: As a developer, manufacturer, and supplier of essential ... Enter and verify data in electronic systems (e.g., LIMS, TrackWise, Veeva ). * Support preparation ...

Quality Auditing Specialist

Corning, NY · On-site

$80K - $110K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Trackwise Travel requirements: 50% + This position does not support immigration sponsorship. The range for this position is $80,011.00 - $110,016.00 assuming full time status. Starting pay for the ...

Specialist, QA SAP

Spokane, WA · On-site

$31 - $41.94/hr

  • Medical

  • Dental

  • Vision

  • Life

High computer aptitude Proficiency in TrackWise and Master Control (SOP and SPEC revisions ... Spokane, WA - On Site, Full- -Time Shift: Monday-Friday Compensation & Benefits That Start on Day ...

Quality Audit Technician

Corning, NY · On-site

$58K - $80K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Trackwise) This position does not support immigration sponsorship. The range for this position is $58,236.00 - $80,075.00 assuming full time status. Starting pay for the successful applicant is ...

Quality Audit Technician

Corning, NY · On-site

$58K - $80K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Trackwise) This position does not support immigration sponsorship. The range for this position is $58,236.00 - $80,075.00 assuming full time status. Starting pay for the successful applicant is ...

Stability Administrator

Bedford, OH · On-site

$44K - $74K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Bedford, Ohio Job Type: Full-Time About Us: As a developer, manufacturer, and supplier of essential ... Enter and verify data in electronic systems (e.g., LIMS, TrackWise, Veeva ). * Support preparation ...

Quality Auditing Specialist

Durham, NC · On-site

$80K - $110K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Trackwise Travel requirements: 50% + This position does not support immigration sponsorship. The range for this position is $80,011.00 - $110,016.00 assuming full time status. Starting pay for the ...

Experience using Trackwise (Event Tracking System) Change Request and Investigation Writing ... Repetitive motion and substantial movement of the wrists, hands, and/or fingers. Full time Regular ...

Showing results 41-60

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 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.

Team Leader - Fermentation

- Zoetis Belgium S.A.

Charles City, IA • On-site

Full-time

Posted 9 days ago


Job description

Role Description

Job Description:

This 2nd shift Team Leader in Fermentation is responsible for the safe execution of the Charles City production schedule in accordance with Good Manufacturing Practices and other applicable regulatory requirements. Team Leaders actively promote colleague engagement and development utilizing both site and corporate resources. Conducts all activities and makes decisions that are in accordance with Company policies & SOPs, Zoetis Values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines as appropriate, etc. Update and maintain department procedures including Manufacturing Directions and SOPs using Microsoft Word software.

Position Responsibilities:

  • Manage and own department performance, including leadership and/or participation in floor operations, area audits, department meetings, shift changes, etc.
  • Must be flexible in daily start time to ensure leadership coverage across the 3-shift operation. Must be available for on-call support in evenings, nights, and weekends.
  • Ensure effective utilization of the GMP process for all direct reports, including annual objectives, individual development plans, one-on-one meetings, quarterly and year-end reviews. Continuously improving the capabilities of the team.
  • Perform safety related M1 investigations, including initial safety event summary to site leadership.
  • Perform manufacturing related M1 investigations as needed in the area.
  • Ensure direct reports are compliant with all training requirements.
  • Perform Human Performance Evaluation as applicable.
  • Continuously develop direct reports to build a strong team and site. This includes the use of performance management tools, improvement initiatives, direct feedback, and open communication.
  • Effective and timely management of employee relations in accordance with company policies and procedures.
  • Participate and/or lead special projects as directed by area Manager/Others.
  • Respond to process and/or equipment events by ensuring communication with process specialists, quality, regulatory, EHS, finance, maintenance, and Operational Excellence specialist(s) as necessary.
  • Compliance and execution of EHS-regulations (Zoetis, US). Compliance and execution of standards and instructions of company manufacturing specifications and SOPs.
  • Responsible for completion of Manufacturing Batch Record Review and other application department documentation.
  • Department Specific Responsibilities as indicated.

Education and Experience:

  • BA/BS with 2-4 years of leadership experience OR MBA/MS with 0-2 years of leadership experience OR Minimum of 8 years relevant leadership experience, preferably in a Biologics manufacturing site.
  • Relevant manufacturing or analytical experience in microbiology, biology, engineering, or other scientific discipline. Demonstrated commitment to the Zoetis Core Beliefs and leadership competencies.
  • Demonstrated ability to effectively lead, develop, and motivate individuals and teams.
  • Demonstrated ability to interact positively with all levels of colleagues including senior leadership.
  • Demonstrated ability to achieve results.
  • Extensive knowledge and capabilities with Microsoft Office software including Word, Excel, and PowerPoint
  • Extensive knowledge and capabilities with SAP Enterprise Resource System
  • Strong communication (oral and written), interpersonal, and team/group interactive and leadership skills.
  • Strong commitment to product quality, customer service, and continuous improvement.
  • Ability to resolve technical issues, troubleshoot manufacturing processes, and investigate process deviations/excursions.
  • Thorough knowledge of 9CFR and EU regulations, Good Manufacturing Practices (GMPs), and Good Laboratory Practices (GLPs).
  • Experience using Trackwise (Event Tracking System) Change Request and Investigation Writing software preferred but not required.
  • Experience using Operational Excellence and problem-solving tools such as DMAIC and Minitab analytical software preferred but not required.
  • Proficient in English, both oral and written, with sound technical writing skills.

Physical Requirements:

  • Must be able to walk, sit, or stand for long periods of time.
  • Must be able to wear a respirator.
  • Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.
  • Must be able to work scheduled 40 hours with the ability to work overtime as needed.
  • Must be comfortable working in varying temperatures.
  • Frequent lifting and carrying of 5 to 25 lbs.
  • Regular reaching, bending, stooping, and twisting.
  • Repetitive motion and substantial movement of the wrists, hands, and/or fingers.
Full timeRegularColleague

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Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.