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Full Time Trackwise Jobs (NOW HIRING)

Eli Lilly and Company

NC · On-site

Experience with TrackWise Deviation and Change Management processes * Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or ...

Lonza

Senior Quality Program Specialist

Walkersville, MD

$95K - $153K/yr

The full-time base annual salary for this position is expected to range between $95,000 to $153,000 ... Perform quality system activities within DMS, LIMS, and TrackWise (Change Control, CAPA, Deviations ...

Lonza

Senior Quality Program Specialist

Walkersville, MD · On-site

$95K - $153K/yr

The full-time base annual salary for this position is expected to range between $95,000 to $153,000 ... Perform quality system activities within DMS, LIMS, and TrackWise (Change Control, CAPA, Deviations ...

Lancesoft

Quality Engineer

Fair Lawn, NJ · On-site

$25/hr

... in quality management software (TrackWise, SAP QM, etc.) and Microsoft Office suite • ... At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are ...

Eli Lilly and Company

NC · On-site

SAP, TrackWise, etc.) * Previous work with combination products or devices with experience with US ... The anticipated wage for this position is $18.02 - $38.61 Full-time equivalent employees also will ...

Eli Lilly and Company

NC · On-site

SAP, TrackWise, etc.) * Previous work with combination products or devices with experience with US ... The anticipated wage for this position is $18.02 - $34.90 Full-time equivalent employees also will ...

Eurofins

Analytical Chemist

Indianapolis, IN · On-site

UV * Smart Lab and Trackwise software experience a plus Qualifications * Strong computer ... The position is full-time, Monday through Friday, 8am-5 pm * May be requested to work on weekends ...

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How much do full time trackwise jobs pay per month?

As of Jun 6, 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 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.

Quality Assurance Project Manager-Bioscience

Smithfield Foods, Inc.

Cincinnati, OH • On-site

Full-time

Posted 12 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 Senior Quality Assurance Manager -a position that sits at the heart of our mission to deliver products that meet the highest global standards.
As the Quality Assurance Projects Manager, 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 Projects Manager Leadership
  • Ensure Site Quality Objectives are met and the Site remains in a state of compliance with all applicable regulations
  • In supplying Quality oversight - the WHY as well as the HOW Quality is applied - is central to the role.
  • Own the Stewardship of the Quality Culture within the QA Function as well as the Site. Promote the values of a Learning Organization.
  • Oversee GMP documentation and systems (Trackwise) management.
  • Manage the site GMP training program
  • Oversee the Quality Engineering and CSV activities.
  • Support site GMP supplier management activities.

Document Management and Trackwise
  • Document Management: Maintain the GMP library and document storage for the site.
  • Trackwise: Oversee the Fit for Purpose and Use of Trackwise by the site. Responsible for the site SME for Trackwise.
  • Training: Administer the site GMP training component. Ensure that training records are maintained in Trackwise and are retrievable.
  • Training Plans: Ensure that GMP training plans are in place / in use for all members at the site. Training plans are to be role specific.

Quality Engineering / CSV
  • Quality Engineering: Oversee all aspects of quality engineering - change controls, GMP systems (purified water, HVAC), system drawings, and process / equipment modifications.
  • Maintenance: Assure that calibration and PM programs are up to date and performing as designed. Ensure that appropriate maintenance system tracking tools are in place.
  • Metrics: Track / trending of critical process metrics and ancillary support metrics (ie: EM Heat Maps, purified water quality)
  • Fit for Purpose: Ensure that the facilities are Fit for Purpose through quality engineering assessments. Determine annual recapitalization budgets and planned shutdowns.
  • CSV: Oversee the stewardship of computer system validation across the site including manufacturing and the QC Labs. See that periodic CSV assessments are completed.
  • Inspection Readiness: Support the site's actions for being Inspection Ready. Create action plans for areas and systems needing remediation. Assist in developing / executing the tracking mechanism for Inspection Readiness.

Supplier Management
  • Process Ownership: Provide direction for GMP supplier management as the process owner.
  • Approved Supplier List: Maintain the site's GMP approved supplier list for materials and services.
  • Periodic Review of Suppliers: Direct the annual review of supplier performance and stratification of suppliers based on criticality.
  • Quality Agreements: Track and report on status of Quality Agreements. Provide governance for keeping supplier Quality Agreements up to date.

Skills & Competencies
  • Knowledge / Expertise in Pharmaceutical Manufacturing Processes.
  • Familiarity working with external suppliers and service providers.
  • Tech Proficiency - Experience with digital quality systems like TrackWise Digital or similar platforms as well as maintenance systems like Blue Mountain.
  • Fluency in creating and using metrics to drive results
  • General understanding of CSV / GAMP 5.
  • Coach and mentoring - enhance the skills of the QA staff and Production Operations for GMP fluency. Good Communicator - Strong written and verbal communication skills, essential for working with external parties and cross-team collaboration.
  • 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 an engineering, chemistry, microbiology or other relevant technical field and 5+ years of relevant manufacturing experience, or an equivalent combination of education and experience, required. Advanced experience in the API manufacturing is highly preferred.
  • Proven leadership or project management experience: Minimum 2 years of demonstrated experience in team management/development or project leadership is required, preferably in API pharmaceutical cGMP manufacturing.
  • Candidates with a Master's Degree in a Science or Technical field from an accredited four-year college or university and 3+ years experience in pharmaceutical cGMP manufacturing 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 API manufacturing is strongly preferred.
  • Experience with digital QMS tools (e.g., TrackWise).
  • Strong understanding of data integrity principles (ALCOA+).
  • Strong communication skills, analytical thinking, critical thinking and cross-functional collaboration skills.
  • Preferred: Certified Quality Manager (CQM), Certified Quality Auditor (CQA), or Six Sigma Black Belt are advantageous, Bilingual communication in Mandarin and English, etc.

Salary Range:
$96,000-$144,000
Relocation Package AvailableNo
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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