Regulatory Engineer

CV-Library

Posted on Sep 19, 2024 by CV-Library
Lancaster, Lancashire, United Kingdom
Engineering
Immediate Start
Annual Salary
Full-Time
Regulatory Engineer - Medical Devices - Competitive Salary and Benefits

A rapidly expanding company in Lancaster is seeking a Regulatory Engineer with experience in the Medical Device sector to join their dynamic team.

You will be instrumental in ensuring regulatory compliance across the company's portfolio, helping to bring innovative healthcare solutions to market.

As a Regulatory Engineer, you will compile and update technical documentation, support regulatory submissions, participate in audits with internal and external stakeholders, ensure ongoing compliance with ISO standards, and investigate non-conformities.

Essential experience:

Knowledge of medical device regulations (e.g., ISO 13485)
Experience with product registrations in global markets
Regulatory documentation and technical file management
Prior experience in conducting audits to quality standards Desirable experience:

Hands-on experience in quality management systems (QMS)
Knowledge of medical air filtration and PPE products
Prior experience implementing and upholding health and safety standards If you’re interested in the Regulatory Engineer opportunity and would like further information or are interested in making an application, please contact Luke Ord

Reference: 222353991

https://jobs.careeraddict.com/post/95444168
CV-Library

Regulatory Engineer

CV-Library

Posted on Sep 19, 2024 by CV-Library

Lancaster, Lancashire, United Kingdom
Engineering
Immediate Start
Annual Salary
Full-Time
Regulatory Engineer - Medical Devices - Competitive Salary and Benefits

A rapidly expanding company in Lancaster is seeking a Regulatory Engineer with experience in the Medical Device sector to join their dynamic team.

You will be instrumental in ensuring regulatory compliance across the company's portfolio, helping to bring innovative healthcare solutions to market.

As a Regulatory Engineer, you will compile and update technical documentation, support regulatory submissions, participate in audits with internal and external stakeholders, ensure ongoing compliance with ISO standards, and investigate non-conformities.

Essential experience:

Knowledge of medical device regulations (e.g., ISO 13485)
Experience with product registrations in global markets
Regulatory documentation and technical file management
Prior experience in conducting audits to quality standards Desirable experience:

Hands-on experience in quality management systems (QMS)
Knowledge of medical air filtration and PPE products
Prior experience implementing and upholding health and safety standards If you’re interested in the Regulatory Engineer opportunity and would like further information or are interested in making an application, please contact Luke Ord

Reference: 222353991

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