Director of Quality & Regulatory Affairs at #twiceasnice Recruiting

First Name *

Last Name

Email *

Phone *

Resume *

Will you now, or in the future, require the hiring company to commence (“sponsor”) an immigration case in order to employ you (for example, H-1B or other employment-based immigration case)? *

What's the highest level of education you have completed? *

How many years class I and/or class II med device experience do you have? *

What company does your medical device experience come from, and which device classes are you familiar with? *

How many years of product development, including verification and validation experience do you have? *

How many years of QMS within an ISO 13485 environment experience do you have? *

How many years of regulatory affairs within an ISO 14971 environment experience do you have? *

How many years of CAPA experience do you have? *

How many years of audit experience do you have? *

How many years of risk management under ISO 14971 experience do you have? *

Do you have experience with 510(k) submissions (not required)? *

Our client has budgeted this role for $150,000-$175,000 + Annual Bonus Potential. Does that fall within your salary expectations or what are you seeking to make a move? *

This role is 100% onsite and our client is in the Miami area, just a few minutes from Amelia Earhart Park. Are you able and willing to work onsite each day? If so, how long is your commute? If you are not currently within commuting distance, would you be open to relocating for the right opportunity (relocation assistance is provided)? *

If you have a LinkedIn profile, please share the URL. *

See all the jobs at #twiceasnice Recruiting here: http://twonice.recruiterbox.com/jobs

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