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Trackwise Jobs in Edison, NJ (NOW HIRING)

Ansell

Account Specialist, Customer Service

Iselin, NJ · Hybrid

$50K - $60K/yr

Knowledge of CRM databases (Oracle and/or Fourth Shift), Salesforce and/or Trackwise Digital experience a plus! * Proficiency with MS Office. * Strong communication, organizational and interpersonal ...

Ansell

Account Specialist, Customer Service

Iselin, NJ · On-site

$50K - $60K/yr

Knowledge of CRM databases (Oracle and/or Fourth Shift), Salesforce and/or Trackwise Digital experience a plus! * Proficiency with MS Office. * Strong communication, organizational and interpersonal ...

Rocket Pharmaceuticals

Training Manager

Cranbury, NJ · Remote

$122K - $158K/yr

Experience with configuration and implementation of eQMS / eLMS (such as ZenQMS, Veeva, Trackwise, ComplianceWire etc). * Experience with training content creation and e-learning tools such as ...

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How much do trackwise jobs pay per month?

As of Sep 11, 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 a Trackwise?

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 does a Trackwise specialist do?

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?

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:

Trackwise jobs near you
Infographic showing various Trackwise job openings in Edison, NJ as of September 2026, with employment types broken down into 89% Full Time, 9% Contract, and 2% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $108,476 per year, or $52.2 per hour.

Technical Operations Scientist

Somerset, NJ • On-site

Lupin Pharmaceuticals Inc.
See more jobs at Lupin Pharmaceuticals Inc.external

Full-time

Re-posted 4 days ago

Job description

Overview
Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way.
Responsibilities
The Technical Operations Scientist reports directly to the Head, of Manufacturing Science and Technology and will support the Manufacturing Science and Technology ( MSAT ) team in authoring technical documents required for cGMP operations at the Somerset facility. The Technical Operations Scientist works with cross-functional teams to prepare scientifically sound documents, and compliance with current regulatory and GMP standards. This role is pivotal in facilitating excellence in Good Documentation practices ( GDP's ). The Somerset facility manufactures and packages solid, powder, and liquid dosage form pharmaceuticals.
  • Prepare and maintain detailed Manufacturing Batch Records (MBRs), Packaging Batch Records (PBRs).
  • Prepare Standard Operating Procedures (SOPs) of MSAT operations
  • Author protocols, and reports for scientific experiments, engineering studies and process validations. Run trial batches for new as well as commercial inline launches.
  • Author Standard Operating Procedures (SOP's) for MSAT operations
  • Collect and analyze data of scientific experiments, and commercial batches using statistical tools and methods
  • Support root cause analysis (problem-solving) using lean principles.
  • Create and manage master recipes in SAP for manufacturing and packaging of the products manufactured in the Somerset facility Systematically Organize and manage documents of MSAT in a shared drive
  • Train the staff on master batch records, protocols and SOPs as needed
  • Initiate QMS records such as Change Controls, CAPA's, deviations pertaining to MSAT operations Coordinate with cross-functional departments on timely approval, closure of QMS records
  • Other duties as assigned

Qualifications
  • Bachelor's or master's Degree in a scientific discipline.
  • 3+ years' experience in benchwork or technical writing for a life science or pharmaceutical organization
  • Must have excellent grammatical skills and effective oral and written communication skills.
  • Adaptable to changes in work duties, responsibilities, and requirements and can manage the workload.
  • Strong interpersonal skills; capability to work as part of a team with formulation scientists and other departments.
  • Working knowledge of SAP, Microsoft Office Suite, Electronic QMS Systems like :- TrackWise, Veeva, etc.
  • Detail-oriented, thorough, and methodical, and excellent organizational and planning skills with the ability to manage and prioritize multiple tasks while still meeting deadlines. Possesses good editorial/proofreading skills and understands and performs well in the process of writing (outlining, drafting, revising, and reviewing).
  • Excellent organizational skills.
  • Able to perform numerous simple and complex tasks without losing sight of overall objectives.
  • Highly Proficient in Word, PowerPoint, and Excel.
  • The position requires proficient personal computer skills including electronic mail; record keeping, routine database activity, word processing, spreadsheet, and graphics.

Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran's status, or any other classification as required by applicable law.
The anticipated annual base salary range for this position in New Jersey is $70,000 to $95,000, plus a discretionary performance bonus (based upon eligibility). The final salary offered to a successful candidate may vary and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, the type and length of experience within the industry, skillset, education, business needs, etc. Lupin is a multi-state employer, and this salary range may not reflect positions that work in other states
Physical Requirements
The physical requirements of the position generally include: standing, walking, sitting, using hands and fingers, reaching with hands and arms, talking and hearing. In some circumstances, bending, kneeling, crouching, stooping, and crawling may apply. This position may require lifting up to 15 pounds occasionally. Generally work is performed in a maniufacturing environment.
Search Firm Representatives Please Read Carefully
Lupin USA, and its Affiliates does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms for any current openings at our company without a valid written search agreement in place will be deemed the sole property of Lupin. No fee will be paid in the event a candidate is hired by Lupin as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, No phone calls or emails

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