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The Role:
An industry-leading medical device manufacturer is seeking an RA consultant based in Berlin.
My client is currently searching for an RA consultant to work in a 6-month project on the activation of nanoparticles, starting at the end of March. The company is an industry-leading manufacturer.
Responsibilities:
-Provide support for currently required products and registration with distributors
-Collating information for what is needed for global regulatory registrations
-Maintenance of regulatory files
-To ensure the compliance of documented information with the applicable standards and internal regulation
-Support the business units and functions in creating, implementing and maintaining processes and the related documented information
Skills and Experience Required
-Strong regulatory background (essential)
-Biomedical / Mechanical / Electrical engineering background (preferred)
-MDR experience
-Thorough understanding of single devices
-Fast learner: there is a vast amount to learn on site
-Knowledge of MDD and AIMDD (preferred)
-Knowledge and experience with 60601 (preferred)
-Experience working with Class lll / Class llb / Class l Software
-Experience with electrical equipment's; MRI, CTs
What this Job Offers You
-Potential for home-based flexibility
-Opportunity to develop invaluable knowledge in
-Competitive rate
How to apply
Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact: enquiries@epmscientific.com or phone +4930726211435
Disclaimers if necessary: Must have the rights to Work in Germany.
RA Consultant
- Location England
- Job type Contract
- Salary Negotiable
- Discipline Regulatory
- Reference CR/250256_1581088348
An industry-leading medical device manufacturer is seeking an RA consultant based in Berlin.
My client is currently searching for an RA consultant to work in a 6-month project on the activation of nanoparticles, starting at the end of March. The company is an industry-leading manufacturer.
Responsibilities:
-Provide support for currently required products and registration with distributors
-Collating information for what is needed for global regulatory registrations
-Maintenance of regulatory files
-To ensure the compliance of documented information with the applicable standards and internal regulation
-Support the business units and functions in creating, implementing and maintaining processes and the related documented information
Skills and Experience Required
-Strong regulatory background (essential)
-Biomedical / Mechanical / Electrical engineering background (preferred)
-MDR experience
-Thorough understanding of single devices
-Fast learner: there is a vast amount to learn on site
-Knowledge of MDD and AIMDD (preferred)
-Knowledge and experience with 60601 (preferred)
-Experience working with Class lll / Class llb / Class l Software
-Experience with electrical equipment's; MRI, CTs
What this Job Offers You
-Potential for home-based flexibility
-Opportunity to develop invaluable knowledge in
-Competitive rate
How to apply
Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact: enquiries@epmscientific.com or phone +4930726211435
Disclaimers if necessary: Must have the rights to Work in Germany.