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Manufacturing Support Technician

Job in Burlington, Middlesex County, Massachusetts, 01805, USA
Listing for: Vericel Corporation
Full Time position
Listed on 2026-08-22
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Manufacturing & Industrial Operations, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 33000 - 36000 USD Yearly USD 33000.00 36000.00 YEAR
Job Description & How to Apply Below

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Regular Full-Time Burlington, MA, US

7 days ago Requisition

At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).

Position Summary

Join a team that supports the production of life-changing cellular therapies. As a Manufacturing Support Technician, you'll play a critical role in preparing and delivering the materials and equipment needed for manufacturing operations. Working in a state-of-the-art cleanroom environment, you'll help ensure products are manufactured safely, efficiently, and compliantly with quality standards that directly impact patients' lives.

Schedule

This position is onsite Sunday - Thursday from 8-4:30pm i n our new Burlington, MA office.

Responsibilities:
  • Perform sanitization, preparation, and staging of materials, components, consumables, and manufacturing equipment within an ISO Class 7 cleanroom environment in accordance with established SOPs, cGMP requirements, and safety regulations.
  • Operate sanitization equipment and execute processes to ensure materials are available and compliant for manufacturing operations.
  • Prepare, stage, label, and transfer sanitized materials into controlled manufacturing environments following approved procedures.
  • Support the development and execution of daily, weekly, and monthly sanitization scheduling.
  • Document and review sanitization and material preparation activities in logbooks, and other controlled documentation in compliance with cGMP requirements.
  • Review completed documentation for accuracy, completeness, and compliance with cGMP and procedural requirements.
  • Maintain accurate records of sanitization cycles, equipment usage, and material traceability.
  • Support inventory management and material flow activities to ensure timely availability of materials for manufacturing.
  • Partner with Manufacturing, Engineering, Facilities, Materials Management, Quality Assurance (QA), Quality Control (QC), Validation, Process and Analytical Development, and other cross-functional teams to ensure efficient and compliant manufacturing operations.
  • Identify and elevate equipment, process, quality issues, or continuous improvement initiatives to improve quality and efficiency.
  • Work independently with general supervision while effectively prioritizing tasks in a dynamic manufacturing environment.
  • Demonstrate strong organizational skills, attention to detail, and the ability to work collaboratively within a team-based setting.
  • Practice safe work habits and comply with all company safety policies, procedures, and training requirements.
  • Perform other duties as assigned.
Basic Qualifications:
  • GED or equivalent with 2+ years of cGMP experience.
  • Excellent communication skills, written and verbal.
  • Organizational and planning skills and the ability to cooperate effectively with others in a team environment.
  • Experience with Microsoft Office.
Preferred Qualifications:
  • Experience working in an ISO 7 cleanroom environment
  • Manufacturing, pharmaceutical, biotechnology, medical device, warehouse, laboratory, or regulated industry experience preferred.
Working Conditions & Physical Demands:
  • Must be able to stand for up to stand for up to 4+ hours.
  • Must be able to lift, carry, push, and pull up to 50 lbs.
  • Ability to work 1 weekend day per week.
  • Rotating holiday coverage.
  • Ability to gown and gain entry to manufacturing areas
Why Vericel?
  • Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care.
  • Career Growth: Be a part of a growing organization with opportunities to expand your impact
  • Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives.

The hourly wage range Vericel reasonably and in good faith expects to pay for this position at…

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