Risk Management Medical Device Expert

Switzerland  ‐ Onsite
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Description

RESPONSIBILITIES:



Tasks and responsibilities would include:



- Lead specific risk management activities within projects, as agreed with project leaders

- Facilitate development and completion of risk assessments.

- Ensure timely completion and quality of the assigned risk management files.

- Manage the overall Risk Management Program of the packaging and device development activities for within the team.

- Ensure compliance with ISO 14971 in all development projects under responsibility of our team.

- Supervise risk management activities in all development projects under responsibility of our team.

- Harmonize the medical device risk management outputs across all development projects under responsibility of our team.

- Supervise and train junior experts and other team members on Risk Management in line with local procedures and regulatory standards.

- Conduct and provide guidance on the use of risk analysis for Use, Products, Components and Processes.

- Ensure compliance with regulatory and normative guidelines focusing on medical device risk management

- Shape and improve the current internal risk management process for medical devices Guide internal and external functions on creating, reviewing and approving medical device Risk Management Files.

- Work with device development team to incorporate and complete Risk Management during all design phases for new and/or product enhancements.

- Apply FDA CFR 820, ISO13485, and ISO 14971 Risk Management in assigned projects.



REQUIRED EXPERIENCE



- 2-3 years of experience as medical device risk management team leader

- Experience in managing risk management files

- Good training and presentation skills

- Good technical knowledge of parenteral packaging and medical devices

- Awareness of Human Factors Engineering

- Development and documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects

- Experience of managing external suppliers

- Excellent skills in English language
Start date
n.a
From
Quanta Consultancy Services
Published at
07.12.2015
Contact person:
Lee Mitchell
Project ID:
1032789
Contract type
Freelance
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