Medical Device Assembly Specialist II – Precision & Impact

Rhevera Medical

Santa Rosa (CA)

In loco

USD 30.000 - 34.000

Tempo pieno

15 ore fa
Candidati tra i primi

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Vantaggi offerti da questo lavoro

Competitive pay
Solid benefits
Career growth
Flexible work-life balance

Descrizione del lavoro

Endologix LLC in Santa Rosa, CA is seeking a Manufacturing Associate II to join our production team. You will assemble high-quality medical devices in accordance with approved processes and assist in solving line issues.

The role requires 2–4 years in regulated life sciences, cleanroom experience, GMP/ISO 13485 knowledge, and precise documentation. We offer competitive pay, benefits, and opportunities for growth in a collaborative environment.

Competenze

  • High school diploma or GED required.
  • Associate degree in life sciences, engineering, or related field preferred.
  • Additional coursework or certification in medical device manufacturing, GMP, or quality systems is a plus.

Mansioni

  • Follow safety guidelines and GMP/GDP practices to ensure a safe and compliant workplace.
  • Assemble products using hand tools, calibrated instruments, microscopes, and fixtures with precision.
  • Identify and communicate safety, quality, or process concerns promptly.
  • Maintain cleanroom integrity with proper attire and procedures.
  • Perform in-process quality checks and provide timely feedback.
  • Document activities in DHRs and ensure traceability.

Conoscenze

GMP/ISO 13485
SOP compliance
Hand tools use
Cleanroom protocols
Documentation in DHRs
ERP/MES experience
MS Office skills
Team collaboration
Problem solving
Training others
Flexible shift work

Formazione

High school diploma or GED
Associate degree in life sciences/engineering
GMP/quality systems certification

Strumenti

ERP/MES systems

Descrizione del lavoro

Endologix LLC in Santa Rosa, CA is seeking a Manufacturing Associate II to join our production team. You will assemble high-quality medical devices in accordance with approved processes and assist in solving line issues.

The role requires 2–4 years in regulated life sciences, cleanroom experience, GMP/ISO 13485 knowledge, and precise documentation. We offer competitive pay, benefits, and opportunities for growth in a collaborative environment.

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