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Senior Manufacturing Technician

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: JCW Group
Contract position
Listed on 2026-01-12
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 26 - 35 USD Hourly USD 26.00 35.00 HOUR
Job Description & How to Apply Below

3 days ago Be among the first 25 applicants

This range is provided by JCW Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$26.00/hr - $35.00/hr

Manufacturing Operations Senior Technician

Type: 6-Month Contract-to-Hire

Job Summary

We are seeking a Manufacturing Operations Senior Technician to support lab-based manufacturing and process development activities related to tissue used in a structural heart medical device. This role is hands‑on and focused on executing established processes, supporting development efforts, and maintaining compliance with GMP requirements for sterile medical device manufacturing.

The ideal candidate has experience working in regulated manufacturing or lab environments, is comfortable following detailed procedures, and collaborates effectively with Engineering, Quality, and Regulatory teams.

Responsibilities
  • Execute lab‑based manufacturing and process development activities supporting tissue processing of mammalian pericardium
  • Perform production runs and follow established work instructions, protocols, and SOPs
  • Support process improvements by identifying issues, documenting observations, and providing input to engineering and development teams
  • Assist with the development and maintenance of tissue‑specific manufacturing procedures and in‑process controls
  • Accurately document manufacturing activities in compliance with GMP requirements
  • Communicate clearly with cross‑functional partners including R&D, Quality, and Regulatory Affairs
Additional Responsibilities
  • Support continuous improvement initiatives within manufacturing and process development
  • Assist with preparation and review of technical documentation such as protocols, reports, and development records
  • Perform additional tasks as assigned to support manufacturing operations
Education, Experience & Skills
  • 3–5 years of experience in manufacturing or laboratory environments within a regulated industry
  • Experience working under GMP, FDA QSR, or ISO 13485 preferred
  • Prior experience with tissue processing or mammalian biological materials strongly preferred
  • Strong attention to detail and ability to follow written procedures
  • Effective written and verbal communication skills
  • Ability to work collaboratively in cross‑functional teams
Physical &

Work Environment Requirements
  • Ability to work in a fast‑paced, hands‑on manufacturing or lab environment
  • Willingness and ability to work in cleanroom settings
  • Comfortable handling mammalian tissue and working with biological materials
  • Ability to manage multiple tasks while maintaining quality and compliance
Authority & Responsibility
  • Responsible for executing assigned manufacturing and process development tasks related to tissue production
  • Accountable for following approved procedures and maintaining accurate documentation
  • Works under the direction of engineering or senior technical staff to support product quality and patient safety
Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Manufacturing

Industries

Medical Equipment Manufacturing

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Position Requirements
10+ Years work experience
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