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Trackwise Jobs in Massachusetts (NOW HIRING)

Astrix Inc

CSV Specialist

Lexington, MA · On-site

$45 - $52/hr

Experience with TrackWise, Veeva, Kneat, ALM, or similar documentation systems. * Familiarity with MODA, LabWare, or other QC/LIMS platforms preferred. * Proficient in Microsoft Teams and electronic ...

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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 are popular job titles related to Trackwise jobs in Massachusetts?

For Trackwise jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Trackwise jobs in Massachusetts look for?

The top searched job categories for Trackwise jobs in Massachusetts are:

What cities in Massachusetts are hiring for Trackwise jobs?

Cities in Massachusetts with the most Trackwise job openings:

Trackwise jobs near you
Infographic showing various Trackwise job openings in Massachusetts as of August 2026, with employment types broken down into 91% Full Time, 8% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution.

Bioprocess Manufacturing Associate - Upstream/Downstream

SOKOL GxP Services

Devens, MA • On-site

$25.70 - $30.70/hr

Contractor

Medical, Dental, Vision, Retirement

Posted 25 days ago

Job description

We are seeking a Bioprocess Manufacturing Associate to support GMP-regulated biotechnology manufacturing operations in Devens, Massachusetts.

The associate will perform upstream or downstream manufacturing activities, including weighing raw materials, assembling and cleaning process equipment, sterilizing equipment, monitoring processes, completing electronic work instructions, and maintaining a compliant cleanroom environment.

The role may involve media and buffer preparation equipment, bioreactors, harvest equipment, chromatography skids, membrane operations, column packing systems, DeltaV, Syncade, OSI PI Historian, SAP, TrackWise, and Maximo.

Position details:

  • Hourly rate: $25.70–$30.70
  • Contract length: 6 months
  • Location: Devens, Massachusetts
  • Work arrangement: 100% onsite
  • Maximum hours: 40 hours per week
  • Rotating schedule includes weekdays, weekends, and scheduled holidays
  • W-2 contract position
  • No C2C options

Requirements

Required:

  • High school diploma or equivalent;
  • At least one year of process operations experience in a highly automated, GMP-regulated biotechnology manufacturing facility;
  • Strong knowledge of upstream and/or downstream unit operations;
  • Practical knowledge of GMP requirements and Standard Operating Procedures;
  • Experience operating bioprocess manufacturing equipment;
  • Ability to follow written procedures and recognize deviations from accepted practices;
  • Experience completing electronic work instructions and manufacturing documentation;
  • Proficiency with common computer, spreadsheet, and web-based applications;
  • Strong attention to detail, accountability, teamwork, and interpersonal skills;
  • Availability for the rotating schedule, including weekends and holidays;
  • Ability to work in a position that handles hazardous materials;
  • Authorization to work in the United States without visa sponsorship.

Preferred:

  • Bachelor’s degree in science, engineering, biochemistry, or a related discipline;
  • Experience with DeltaV, Syncade, OSI PI Historian, SAP, TrackWise, or Maximo.

Benefits

  • Health insurance with dental and vision insurance options.
  • Holiday pay.
  • 401(k) program.
  • Employee referral bonus program.
  • Six-month W-2 contract with possible extension.
  • Client retains the right to hire the contractor directly.