Lead Specialist, Quality Engineer

at  GE Healthcare

Uusimaa, Etelä-Suomi, Finland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Jan, 2025Not Specified19 Oct, 2024N/ARoot Cause,English,Regulatory Requirements,IsoNoNo
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Description:

JOB DESCRIPTION SUMMARY

We are looking for a Lead Specialist, Quality Engineer. The Lead Specialist, Quality Engineer is responsible for providing process support for our engineering and production teams in accordance with our procedures & practices. This is a key technical role responsible for the continuous development, implementation and reinforcement of our quality assurance practices. Lead Specialist, Quality Engineer is also a core member in design development and production teams engaged in development and production of high-quality medical device systems.

QUALIFICATIONS AND REQUIREMENT

  • Bachelor’s degree or advanced degree
  • Experience in Quality Assurance, Quality Engineering or Production Quality in medical device industry
  • Demonstrated understanding of medical device QMS requirements and regulatory requirements, including but not limited to FDA CFR 21 820 and ISO 13485
  • Demonstrated understanding of medical device design control requirements
  • Demonstrated understanding of medical device production control requirements
  • Demonstrated knowledge of Quality and Process Improvement tools
  • Ability to communicate effectively in Finnish and English

DESIRED SKILLS

  • Strong technical aptitude
  • Ability to handle tasks with competing priorities effectively
  • Demonstrated collaboration and conflict resolution skills
  • Analytical, problem solving and root-cause analysis skills
  • Change agent with energy, passion and enthusiasm to drive change

Responsibilities:

  • Ensures quality and regulatory compliance in accordance with documented procedures
  • Leads development and implementation of strategy to ensure compliance and product quality
  • Ensures process efficiency and compliance
  • Drives, influences and supports continuous process improvement
  • Drives, influences and supports continuous product quality improvement
  • Supports CAPA process
  • Performs internal audits and supports external audits


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Uusimaa, Finland