Lead Specialist, Quality Engineer
at GE Healthcare
Uusimaa, Etelä-Suomi, Finland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Root Cause,English,Regulatory Requirements,Iso | No | No |
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Full Time | Part Time |
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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