Sterilization Technician I - Cleanroom, ISO 13485, GMP

Phiex Technologies

State College (Centre County)

On-site

USD 42,000 - 65,000

Full time

12 days ago

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Benefits offered by this job

Competitive Wage
Insurance: Healthcare, dental, and vis
401(k) program with employer match
Public & Legal Holidays (11)

Job summary

Phiex Technologies seeks a Technician I to join a fast-paced lab and assembly environment at our State College facility. You will assemble sterilization products, utilize hand and power tools, and operate automated equipment, all while maintaining strict quality programs and documentation.

Your role supports ongoing R&D and production initiatives, with emphasis on ISO 13485 compliance, GMP practices, and accurate data capture. Travel may be required as projects evolve.

Qualifications

  • The Technician I is experienced in a fast-paced technical environment and possesses excellent communication and interpersonal skills.
  • Experience Preferred: 1 to 3 years.
  • Demonstrates ability to work with others in a team environment.
  • Strong reading comprehension and attention to detail.

Responsibilities

  • Assemble parts and products using hand tools, power tools, and automated machinery.
  • Maintain quality standards (including ISO 13485) and Good Documentation Practices.
  • Record production data and test results in logs or software.
  • Follow SOPs and GMP while working in a cleanroom environment.
  • Identify defects or contamination and troubleshoot assembly issues.

Skills

Excellent communication
Attention to detail
Hand-eye coordination
Team player

Education

Technical degree or B.S.

Job description

Phiex Technologies seeks a Technician I to join a fast-paced lab and assembly environment at our State College facility. You will assemble sterilization products, utilize hand and power tools, and operate automated equipment, all while maintaining strict quality programs and documentation.

Your role supports ongoing R&D and production initiatives, with emphasis on ISO 13485 compliance, GMP practices, and accurate data capture. Travel may be required as projects evolve.

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