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Trackwise Qms Jobs (NOW HIRING)

Proficiency with QMS platforms including Trackwise, SAP, Coupa and Agile for supplier file management, SCAR tracking, and audit scheduling. * Proficiency with MS Office suite; working knowledge of ...

Proficiency with QMS platforms including Trackwise, SAP, Coupa and Agile for supplier file management, SCAR tracking, and audit scheduling. * Proficiency with MS Office suite; working knowledge of ...

Proficiency with QMS platforms including Trackwise, SAP, Coupa and Agile for supplier file management, SCAR tracking, and audit scheduling. * Proficiency with MS Office suite; working knowledge of ...

Proficiency in relevant technology such as Veeva QMS, Oracle Agile QMS, Trackwise, Smartsheet, MS Project, Visio, PowerPoint and MS Office for efficient project administration and implementation.

Experience with enterprise QMS platforms such as ETQ Reliance, Veeva Vault QMS, MasterControl, TrackWise, or ComplianceQuest. * Experience working in regulated industries such as life sciences ...

GMP Technical Writer

Kenosha, WI · On-site

$60 - $75/hr

... or TrackWise • Strong understanding of GMP documentation principles (data integrity, version ... QMS frameworks • Exposure to legacy site remediation or quality system transition projects • ...

Experience working with document or quality management systems such as MasterControl, Veeva, TrackWise, SharePoint, or similar platforms. * Familiarity with regulated environments such as life ...

Experience working with document or quality management systems such as MasterControl, Veeva, TrackWise, SharePoint, or similar platforms. * Familiarity with regulated environments such as life ...

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Trackwise Qms information

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$30

$56

$92

How much do trackwise qms jobs pay per hour?

As of Jun 18, 2026, the average hourly pay for trackwise qms in the United States is $56.81, according to ZipRecruiter salary data. Most workers in this role earn between $38.70 and $65.62 per hour, depending on experience, location, and employer.

What is the difference between Trackwise Qms vs Quality Assurance Specialist?

AspectTrackwise QmsQuality Assurance Specialist
CertificationsISO 9001, GMP, GxPISO 9001, Six Sigma, GMP
Work EnvironmentQuality management systems, software platformsLaboratories, manufacturing plants
Industry UsagePharmaceuticals, biotech, medical devicesManufacturing, healthcare, pharma

Trackwise Qms focuses on managing quality processes through software platforms, ensuring compliance and documentation. A Quality Assurance Specialist performs inspections, audits, and ensures product quality on the ground. While both roles aim to uphold quality standards, Trackwise Qms professionals manage systems and workflows, whereas Quality Assurance Specialists execute hands-on quality checks.

What are the key skills and qualifications needed to thrive as a TrackWise QMS Specialist, and why are they important?

To thrive as a TrackWise QMS Specialist, you need a solid understanding of quality management systems, compliance regulations (like FDA, ISO), and experience with TrackWise software, often supported by a degree in life sciences, engineering, or a related field. Proficiency in configuring and maintaining the TrackWise platform, understanding workflows, and familiarity with data analysis tools are highly valued, with certifications in TrackWise or QMS being advantageous. Strong problem-solving, communication, and project management skills enable effective collaboration and issue resolution across departments. These skills ensure the organization maintains regulatory compliance, optimizes quality processes, and successfully leverages TrackWise to improve operational efficiency.

What are some typical challenges faced by professionals working with TrackWise QMS, and how can they be addressed?

Professionals working with TrackWise QMS often encounter challenges such as adapting to frequent software updates, managing complex workflows, and ensuring data integrity across quality processes. Staying up-to-date with the latest TrackWise features and participating in regular training sessions can help mitigate these issues. Additionally, collaborating closely with IT teams and end-users ensures smooth implementation and effective troubleshooting, making it essential to cultivate strong communication and problem-solving skills in this role.

What is a TrackWise QMS?

TrackWise QMS is an enterprise quality management software developed by Sparta Systems, designed to help organizations manage quality and compliance processes. It streamlines tasks like document control, corrective and preventive actions (CAPA), audits, and complaints management. The platform is widely used in regulated industries such as pharmaceuticals, biotechnology, and manufacturing to ensure compliance with industry standards and regulatory requirements. By centralizing quality data and automating workflows, TrackWise helps organizations reduce risk, improve efficiency, and maintain product quality.
Infographic showing various Trackwise Qms job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $118,171 per year, or $56.8 per hour.
Sr. Director Quality Systems

Sr. Director Quality Systems

Becton, Dickinson and Company

San Diego, CA • On-site

Full-time

Posted 27 days ago


BD rating

7.2

Company rating: 7.2 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

268th of 418 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
We are the makers of possible!
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us.
This role will lead all aspects of the Medication Management Solutions (MMS) entities, including but not limited to, San Diego and Tijuana, to seek quality system harmonization across the entities and to drive these systems to meet changing regulatory demands (e.g., MDR, QMSR).
Drive the design, development, and implementation of these QMS processes with corporate and business objectives. In some cases, the actual ownership of these processes will be by other MMS QA leaders.
Complete the integration of the MMS QMS into the larger BD QMS and Inspire Quality (IQ) initiatives. Drive the MMS QMS upgrade project that seeks to achieve compliance with EUMDR and seeks to drive QMS efficiency and effectiveness. Act as the point person for internal and external audits and inspections, with organizational skills and strong communication to regulatory agencies. Coordinate external MMS communications with regulators to establish consistency and trust. Act as the point of contact for internal and external audit actions.
Responsibilities:
Drive MMS Quality Systems strategy as follows:
  • Compliance - Ensure compliance with global regulatory standards for medical devices and non-medical devices across various physical locations and entities.

  • Effective and efficient Quality Management - Ensures the MMS QMS is efficient, compliant and simplified to promote the best quality practices.

  • Leadership - Leads or influences quality networks, businesses, associates and capital resources toward the effective promotion and alignment of organizational goals to the company's mission and vision. Demonstrates strong big-picture thinking; effectively integrates and balances long-term opportunities and challenges, with day-to-day activities. Understands implications of decisions and communications both written and verbal.

  • Innovation- The MMS product development process is conducted under the MMS QMS. This QMS must be streamlined to develop new products and change management practices to ensure we deliver a compliant world class customer experience.

  • Growth - Responsible for the effectiveness of the MMS QMS. An effective QMS delivers high performing, safe products that meet and exceed customer expectations.

Qualifications:
  • The candidate should have at least a BS degree in a technical field. Knowledge of industry QMS software tools (e.g., Trackwise, Agile, and Documentum) is desirable
  • A minimum of 12-15 years of experience as either a leader or senior leader of QA in a site/business unit having broad responsibility for QMS process, or as a leader responsible for a corporate wide QMS in a highly matrixed global organization.

  • Must be willing to travel and engage MMS entities worldwide to understand their needs and develop QMS processes that meet those needs.

  • Knowledge of industry QMS software tools (e.g., Trackwise, Agile, and Documentum) is strongly desirable.

  • Excellent verbal and written communication skills and have an ability to influence others within and external to the organization.

  • Experience developing a long-term strategy for the MMS QMS and be able to fulfill this strategy.

  • Experience managing staff, developing future quality leaders and building an organizational culture is required

  • Effectively operates in a matrix environment and influence and interact with senior enterprise leaders and functional leaders on a regular basis is required
  • Demonstrated success leading cross-functional development, implementation, application, maintenance, and continuous improvement of Quality Systems for medical devices (including CAPA, Change Control, Document Control, Post Market Surveillance, Supplier Controls and Internal Audit, as applicable).
  • Demonstrates a solid understanding of what a good QMS process looks like based on experience across multiple companies or business units in a highly matrixed global organization.

  • Demonstrate the ability to develop a QMS that is both compliant and efficient

  • Expert knowledge of applicable regulations and standards including FDA QSR, ISO-13485, EU MDD, and EU MDR

  • Experience leading direct reports

  • Ability to travel and engage MMS entities worldwide to understand their needs and develop QMS processes that meet those needs

  • Certifications within Quality disciplines (i.e. CQE, CSQE, CQA, CQM) strongly preferred

  • Excellent verbal and written communication skills and have an ability to influence others in the organization. They must be able to develop a long-term strategy for the MMS QMS and be able to fulfill this strategy

  • Experience managing staff, developing future quality leaders and building an organizational culture is required

  • Ability to effectively operate in a matrix environment and influence and interact with senior enterprise leaders and functional leaders on a regular basis is required

Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable and learn and improve every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. And through the organization's investment in BD University, you will continually level up your tech skills and expertise.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit https://bd.com/careers
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA CA - San Diego Bldg A&B
Additional Locations
Work Shift
At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."
Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.
Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.
Salary Range Information
$220,300.00 - $352,500.00 USD Annual

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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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