Principal Technician

Abbott

St. Paul, Minnesota, United States
Base: $33.35 – $66.75ph; bonus/equity: not specifi...
Hybrid (based on typical industry practices for technical roles, although not explicitly stated)
7 years medical device industry experience
Fda gmp mdd iso compliance knowledge
Read and create diagrams charts schematics
Abbott is seeking a Principal Technician to support engineers and project teams in product testing and development within the medical device industry in St. Paul, Minnesota. The role involves ensuring compliance with safety and quality standards, coordinating testing workflows, and collaborating with various departments

Job Summary

  • Abbott is a global healthcare leader serving people in more than 160 countries with a portfolio of life-changing technologies.
  • The role requires supporting engineers through concept feasibility to validation while ensuring all documentation meets FDA and ISO standards.
  • Employees qualify for benefits including free medical coverage, a high employer contribution retirement plan, and tuition reimbursement programs.

Matching Summary

Match Score: 85

Abbott is seeking a Principal Technician to support engineers and project teams in product testing and development within the medical device industry in St. Paul, Minnesota. The role involves ensuring compliance with safety and quality standards, coordinating testing workflows, and collaborating with various departments.

Salary

Base: $33.35 – $66.75/hour; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • 7 years medical device industry experience
  • FDA GMP MDD ISO compliance knowledge
  • Read and create diagrams charts schematics
  • Execute test protocols procedures validations
  • Maintain quality records and documentation

Nice-to-have

  • Strong mechanical aptitude for assembly
  • Experience with 3D printing technology
  • Knowledge of DOE test development
  • Catheter guidewire sheath construction skills
  • Leadership skills to prioritize workflow

Key Requirements

  • Minimum 7 years technical experience in medical device industry
  • Vocational or Technical education or equivalent work experience
  • Understanding of FDA QRS GMP MDD and ISO standards

Work Rights

Not specified

Tailored Resume

Cover Letter