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Trackwise Jobs in Edison, NJ (NOW HIRING)

Thermo Fisher Scientific

Sr IT Business Analyst

New York, NY · On-site +1

$94K - $125K/yr

... TrackWise/TrackWise Digital • Advanced knowledge of Agile methodologies and project management practices • Demonstrated ability to manage multiple complex projects simultaneously • Strong ...

System One

Documentation Coordinator

Branchburg, NJ · On-site

$30/hr

SAP, TrackWise, Monday.com) * The need for a candidate who is computer-savvy, possesses strong attention to detail, and understands databases and computer skills. * A background in regulatory ...

WuXi Biologics

QA Specialist I

Cranbury, NJ · On-site

Knowledge of TrackWise and MasterControl is desired. * Knowledge of FDA and EMA regulations, ICH and cGMP guidelines is a plus * Knowledge of Biopharmaceutical manufacturing is desired. * Good Oral ...

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$9K

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How much do trackwise jobs pay per month?

As of Jul 28, 2026, the average monthly pay for trackwise in Edison, NJ is $9,039.67, according to ZipRecruiter salary data. Most workers in this role earn between $5,391.67 and $12,683.33 per month, depending on experience, location, and employer.

What is the highest paid logistics job?

In logistics, senior roles such as Logistics Director or Supply Chain Director tend to be the highest paid, often earning six-figure salaries. These positions require extensive experience, strategic planning skills, and often involve overseeing large teams and complex operations.

What jobs pay 4000 a week without a degree?

High-paying jobs that can reach $4,000 a week without a degree often include roles such as commercial truck drivers, real estate brokers, sales managers, and certain skilled trades like electricians or plumbers. These positions typically require specialized training, certifications, or experience rather than a college degree, and may involve long hours or physically demanding work.

What is the 3 month rule for jobs?

The 3 month rule in the context of jobs, including roles like Trackwise, often refers to a probation or trial period during which an employee's performance is evaluated. During this time, either the employer or employee can typically terminate the employment with minimal notice, and it may influence eligibility for benefits or permanent status. This period helps both parties assess fit before committing long-term.

What does TrackWise do?

TrackWise is a quality management software used by organizations to monitor and manage compliance, quality processes, and regulatory documentation. It helps streamline workflows, track issues, and ensure adherence to industry standards, often requiring knowledge of validation and regulatory requirements. The system is commonly used in regulated industries like pharmaceuticals and biotechnology.

What is a TrackWise job?

A TrackWise job typically involves working with TrackWise, a quality management system (QMS) used in regulated industries like pharmaceuticals, medical devices, and biotechnology. Professionals in these roles manage and configure TrackWise to streamline quality processes such as deviations, CAPA, audits, and complaints. Responsibilities may include system administration, troubleshooting, validation, and ensuring compliance with regulatory standards. Strong knowledge of TrackWise configuration, workflows, and reporting is often required.

What are the typical daily responsibilities of a TrackWise Specialist?

As a TrackWise Specialist, your typical day involves configuring and maintaining the TrackWise quality management system, resolving user issues, and supporting key functions such as CAPA, document management, and audit tracking. You will regularly collaborate with quality assurance, IT, and operations teams to ensure system alignment with company processes and regulatory requirements. Additionally, you may train end-users, generate reports, and participate in system upgrades or process improvement initiatives. This role requires strong attention to detail and excellent communication skills to ensure accurate data management and continuous quality improvement.

What are the key skills and qualifications needed to thrive in the Trackwise position, and why are they important?

To thrive as a TrackWise Specialist, you need a strong foundation in quality management systems (QMS), regulatory compliance knowledge, and experience in data analysis, typically supported by a degree in life sciences, engineering, or a related field. Proficiency in the TrackWise QMS software, as well as familiarity with document control, CAPA, and audit management modules, is essential, and TrackWise certification is highly regarded. Strong problem-solving, attention to detail, and effective communication skills are key soft skills for collaborating with cross-functional teams and troubleshooting system issues. These competencies are critical to maintaining regulatory compliance, optimizing workflow efficiency, and ensuring the successful implementation and support of TrackWise solutions in an organization.

What are popular job titles related to Trackwise jobs in Edison, NJ? For Trackwise jobs in Edison, NJ, the most frequently searched job titles are:
What job categories do people searching Trackwise jobs in Edison, NJ look for? The top searched job categories for Trackwise jobs in Edison, NJ are:
Trackwise jobs near you
Infographic showing various Trackwise job openings in Edison, NJ as of July 2026, with employment types broken down into 56% Full Time, and 44% Contract. Highlights an 100% In-person job distribution, with an average salary of $108,476 per year, or $52.2 per hour.
Investigation Writer / Deviation Investigator

Investigation Writer / Deviation Investigator

Intellectt INC

New York, NY • On-site

Contractor

Posted 17 days ago

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Investigation Writer / Deviation Investigator based in Rensselaer, NY with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com
Role: Investigation Writer / Deviation Investigator
Location: Rensselaer, NY (On-site)
Industry: API Manufacturing
Objective:

  • Drive investigation backlog reduction, improve closure performance, and support timely batch release.

Key Responsibilities:

  • Lead GMP deviation investigations from initiation to closure.
  • Author investigation reports and perform Root Cause Analysis (5 Why, Fishbone, 6M, Cause & Effect).
  • Assess product, process, and batch impact.
  • Define, implement, and verify CAPA effectiveness.
  • Manage investigations and workflows in TrackWise/eQMS.
  • Support backlog remediation and remove investigation bottlenecks.
  • Facilitate cross-functional investigation meetings with QA, QC, Manufacturing, Engineering, Technical Services, Maintenance, and Calibration teams.

Required Experience:

  • Hands-on API Manufacturing experience.
  • GMP deviation and quality event investigation leadership.
  • QC investigations including OOS, OOT, lab deviations, and analytical discrepancies.
  • Strong technical writing and investigation report authoring skills.
  • Experience with CAPA, RCA methodologies, and TrackWise/eQMS.
  • Ability to manage multiple investigations simultaneously.

Ideal Candidate:

  • Self-driven with strong ownership and accountability.
  • Confident in challenging stakeholders professionally.
  • Excellent cross-functional collaboration and communication skills.

Thanks & Regards,
Vyshnavi
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999 - Ext: 225