16 Regulatory Affairs Manager (European Union expertise) Jobs in Tucson, AZ
Talentry is Hiring a Regulatory Affairs Manager (European Union expertise) Near Tucson, AZ
Medical Device Company. Tucson, AZ
140k
Talentry is looking for a Regulatory Affairs expert with medical device experience in the European Union (EM MDR). This expert will aid in the preparation of documentation, submissions, applications, responses, adverse reports, deficiency letter responses, etc., supporting the EU and other international regulatory paradigms.
The best person for this role will prepare documentation, monitor and track control systems, research regulatory issues and trends, etc. He or she will also respond to NCRs, and Quality System deficiencies.
Requirements:
BS or similar, and 6 years of experience.
Proven experience with EU MDR experience.
Excellent communication and documentation experience.
Detail oriented, proactive.
Job Summary
Full Time
$120k-160k (estimate)
05/31/2024
07/30/2024
talentry.net
San Diego, CA
<25
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Quotes from people on Regulatory Affairs Manager job description and responsibilities
Regulatory Affairs Managers plan, direct, or coordinate production activities of an organization to ensure compliance with regulations and standard operating procedures.
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They'll establish regulatory priorities or budgets and allocate resources and workloads.
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Career tips from people on Regulatory Affairs Manager jobs
Having the knowledge and understanding of complex medical and scientific subject matter would give you advantage for this role.
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You need the ability to build networks to obtain cooperation.
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Manager Regulatory Affairs are able to balance projects with day-to-day duties, ensuring participation from other members of the department as needed.
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They utilize their technical skills to ensure products remain safe and efficient by meeting all the regulatory standards.
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You need to have IT skills, particularly in relation to using databases and familiarity with commercial software to qualify for this role.
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