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Full Time Trackwise Jobs (NOW HIRING)

Zoetis, Inc.

Team Lead - TCO

Charles City, IA · On-site

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 ...

Corning

Quality Auditing Specialist

Durham, NC · On-site

$80K - $110K/yr

... 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 ...

Corning

Supplier Service Technician

Durham, NC · On-site

$69K - $96K/yr

... Trackwise) This position does not support immigration sponsorship. The range for this position is $69,880.00 - $96,085.00 assuming full time status. Starting pay for the successful applicant is ...

Corning

Supplier Service Technician

Durham, NC

$69K - $96K/yr

... Trackwise) This position does not support immigration sponsorship. The range for this position is $69,880.00 - $96,085.00 assuming full time status. Starting pay for the successful applicant is ...

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Full Time Trackwise information

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$4.9K

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How much do full time trackwise jobs pay per month?

As of Jul 22, 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 July 2026, with employment types broken down into 74% Full Time, 24% Part Time, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $104,783 per year, or $50.4 per hour.
Senior Quality Assurance Manager - BioScience

Senior Quality Assurance Manager - BioScience

Smithfield Foods, Inc.

Cincinnati, OH • On-site

Full-time

Re-posted 9 days ago

Job description

If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub.
Have a seat at our table. When you join Smithfield, you become part of something special - a company that's sustainably feeding people around the world, producing good food the right way with respect for our people, animals, communities and planet. With opportunities across locations and functions, a culture grounded in our Core Four values - gratitude, communication, respect and accountability - and a strong commitment to learning, collaboration, and innovation, Smithfield offers challenging and rewarding careers where you can grow, contribute and make a real impact. Apply Now!
THE VALUE YOU'LL BRING:
The position summary states the general nature and purpose of the job. Overall accountabilities are defined in this section.
Step Into a High-Impact Role in Quality Assurance!
Ready to make a real difference in the world of pharmaceutical and medical device manufacturing? Smithfield BioScience, Inc. (SBC) is seeking a quality-driven professional for a full-time role reporting to the Head of Quality-a position that sits at the heart of our mission to deliver products that meet the highest global standards.
As a Quality Assurance leader, you'll be on the front lines of enforcing current Good Manufacturing Practices (cGMP) and safeguarding the integrity of our quality management systems. You won't just be checking boxes-you'll be shaping the standards that ensure our FDA-registered facility operates with unmatched precision and compliance.
Your oversight will be critical to the manufacture of high-quality Active Pharmaceutical Ingredients (APIs) and medical device components, all in accordance with 21 CFR Parts 210/211, ICH Q7, ISO 22442, and EU regulatory guidelines. You'll own system controls, uphold procedural excellence, and be a key driver of continuous improvement and operational readiness.
If you're passionate about compliance, thrive in a fast-paced regulated environment, and are ready to lead with confidence-this is the opportunity for you.
WHAT YOU'LL DO:
The below statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. May perform other duties as assigned.
Quality Assurance Leadership
  • Lead and manage the QA team to ensure full compliance with cGMP standards and adherence to internal SOPs.
  • Provide strategic direction and decision-making on all quality-related matters, acting as a go-to leader during escalations.
  • Champion a culture of quality-first thinking, driving operational excellence across departments.

Process Development & Continuous Improvement
  • Collaborate in the design, development, and refinement of quality systems, procedures, and product processes.
  • Drive continuous improvement initiatives across QA operations to streamline workflows and elevate product quality.
  • Coordinate with Regulatory Affairs to assess the impact of critical change control activities on customer satisfaction and compliance.

Data Management & Reporting
  • Ensure accurate recordkeeping, archival, and retrieval of all QA-related data, supporting traceability and audit-readiness.
  • Compile and present quality metrics and key performance indicators (KPIs) to senior management for informed decision-making.
  • Assist in preparation and presentation of the Annual Product Review to the Quality Review Board.

Regulatory Compliance & Inspection Readiness
  • Maintain the facility in a constant state of readiness for FDA, EU, and other regulatory inspections.
  • Actively participate in internal audits, customer audits, and regulatory inspections, demonstrating a deep understanding of applicable standards.
  • Stay current with evolving FDA, EU, and ICH regulations, ensuring company procedures remain aligned with global expectations.

Quality Systems Oversight
  • Oversee and safeguard company Quality Management System (QMS) records to ensure accuracy, security, and compliance.
  • Ensure timely and thorough investigations of OOS (Out of Specification) results, CAPAs, complaints, and deviations, all in accordance with FDA guidelines.
  • Collaborate cross-functionally to support the validation of company processes, test methods, and computerized systems.

Skills & Competencies
  • Detail-Oriented Problem Solver - Able to spot quality issues early and implement smart, sustainable solutions.
  • Exceptional Communicator - Strong written and verbal communication skills, essential for audits, reporting, and cross-team collaboration.
  • QMS & Tech Proficiency - Experience with digital quality systems like TrackWise Digital or similar platforms.
  • Team Player with Leadership Drive - Comfortable managing multiple priorities in a collaborative, fast-paced environment.
  • Analytical Thinker - Brings logic, critical thinking, and data-driven decision-making to every challenge.

WHAT WE'RE SEEKING:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions.
  • Bachelor's degree from an accredited four-year college or university in a chemistry, microbiology or other relevant technical field and 8+ years of relevant manufacturing experience, or an equivalent combination of education and experience, required.
  • Minimum 2 years of demonstrated experience in team management/development or project leadership is required preferably in pharmaceutical cGMP manufacturing.
  • Candidates with a Master's Degree in a Science or Technical field from an accredited four-year college or university and 6+ years relevant experience will be considered qualified.
  • In-depth knowledge of relevant regulations and standards in the pharmaceutical industry (e.g., 21 CFR Part 210/211, ICH Q7, 21 CFR Part 11).
  • Strong understanding of Good Manufacturing Practices (GMP) and their application in the pharmaceutical industry.
  • Experience in developing, implementing, and maintaining a quality management system.
  • Experience in conducting internal and external audits and managing audit programs.
  • Proficient with the TrackWise QMS modules for Quality Events, CAPA, OOS, and Audit (or equivalent eQMS system).
  • Familiarity with risk management principles and tools, including FMEA (Failure Modes and Effects Analysis) and risk assessment methodologies.
  • Excellent analytical, problem-solving, and root cause analysis skills, with the ability to apply data-driven decision-making.
  • Strong written and verbal communication skills, with the ability to effectively interact with cross-functional teams, regulatory authorities, and external stakeholders.
  • Relevant certifications such as Certified Quality Manager (CQM), Certified Quality Auditor (CQA), or Six Sigma Black Belt are advantageous
  • Strong Communicator: Exceptional written and verbal communication skills, capable of articulating complex technical issues clearly and concisely across all levels of the organization. Bilingual communication in Mandarin and English is preferred.

IndSPR-Ops
The expected pay range for this position is $120,000 - $162,500 annually.
Smithfield Foods provides pay ranges that reflect its good faith estimate of the salary or hourly wage the company reasonably expects to pay for a position at the time of hire. Individual compensation will be determined based on several factors, including but not limited to, the scope and responsibilities of the role, location of the position, the candidate's qualifications and experience, internal equity, external market pay for comparable positions and budget considerations. At Smithfield Foods, base pay represents only one aspect of the comprehensive total rewards package. Learn more about our benefits package here.
Relocation Package AvailableYes
EEO Information
Smithfield is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, gender identity, protected veterans status, status as a disabled individual or any other protected group status or non-job characteristic as directed by law.
If you are an individual with a disability and would like to request a reasonable accommodation for any part of the employment selection process, please call us at 757-357-1595.

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