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Trackwise Jobs in Massachusetts (NOW HIRING)

Enter document reviews into Trackwise and maintain up-to-date and accurate Excel documentation. * Support the verification process of all patient records, ensuring completeness, accuracy, and ...

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Enter document reviews into Trackwise and maintain up-to-date and accurate Excel documentation. * Support the verification process of all patient records, ensuring completeness, accuracy, and ...

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Trackwise information

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 cities in Massachusetts are hiring for Trackwise jobs? Cities in Massachusetts with the most Trackwise job openings:
Infographic showing various Trackwise job openings in Massachusetts as of August 2026, with employment types broken down into 81% Full Time, 2% Temporary, 16% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Quality Assurance Technician

Actalent

Cambridge, MA

$30 - $40/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Job description

Job Title: Quality Assurance Technician

Job Description

The Quality Assurance Technician verifies and approves Quality Control (QC) data, reviews batch records, and supports the verification of patient records to ensure compliance with GMP and ISO standards. This role works closely with the QA team to maintain accurate documentation, manage Trackwise entries, and support a growing product line within a regulated pharmaceutical or biotech environment.

Responsibilities

  • Verify and approve Quality Control (QC) data accurately and in a timely manner.
  • Review batch records thoroughly and ensure a complete and accurate chain of custody for all materials and documentation.
  • Enter document reviews into Trackwise and maintain up-to-date and accurate Excel documentation.
  • Support the verification process of all patient records, ensuring completeness, accuracy, and compliance with applicable standards.
  • Perform detailed QC data review and clinical documentation review in alignment with internal procedures and regulatory requirements.
  • Apply knowledge of GMP and ISO standards to daily QA activities and documentation practices.
  • Utilize SAP and D365 to support quality assurance processes, data tracking, and documentation.
  • Contribute to quality assurance testing activities and help identify, document, and escalate quality issues as needed.
  • Collaborate with the QA team to support continuous improvement of quality systems and processes.
  • Ensure all work aligns with established quality procedures, regulatory expectations, and internal policies.

Essential Skills

  • Proficiency in quality assurance and batch record review.
  • Hands-on experience with QC data review and clinical documentation.
  • Demonstrated knowledge of GMP requirements and ISO standards.
  • Experience using Trackwise for document reviews and quality workflows.
  • Ability to maintain and manage Excel documentation accurately.
  • Familiarity with SAP and D365 in a quality or manufacturing environment.
  • Associate or Bachelor of Science (BS) degree in a life science discipline.
  • 1–3 years of relevant pharmaceutical or biotech experience.
  • Strong attention to detail and ability to identify discrepancies in documentation.
  • Ability to work effectively as part of a QA team and follow established procedures.

Additional Skills & Qualifications

  • Very knowledgeable in working under GMP requirements within a regulated environment.
  • Experience with quality assurance testing and related QA activities.
  • Comfort working with electronic quality systems such as Trackwise.
  • Ability to manage multiple documentation tasks and priorities simultaneously.
  • Interest in gaining exposure to new product lines and expanding QA expertise.
  • Strong written and verbal communication skills for clear documentation and collaboration.

Work Environment

The Quality Assurance Technician works 100% within the QA team and follows a Tuesday–Saturday schedule, providing consistent support during core operational days. The role requires regular travel between sites in Cambridge and Burlington, so candidates should be comfortable commuting between these locations as part of their weekly routine. The environment is a regulated pharmaceutical or biotech setting that operates under GMP and ISO standards, using systems such as Trackwise, SAP, D365, and Excel to manage quality documentation and workflows. Team members gain exposure to a new product line and have the opportunity to run a significant portion of QA work, contributing directly to the reliability and compliance of critical processes.

Job Type & Location

This is a Contract position based out of Cambridge, MA.

Pay and Benefits

The pay range for this position is $30.00 - $40.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Cambridge,MA.

Application Deadline

This position is anticipated to close on Aug 7, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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