Job Description
Reporting to the VP-Quality & regulatory Affairs you will be responsible for the global strategy and content of all regulatory issues.Develop a strategic plan and total outlay of the product making sure all validation and verification studies comply with regulatory requirements.Strength of character and intellectual depth a must,outstanding communication skills and be able to articulate clearly in regards to requirements and expectations for the regulatory affairs function.Must have a Bachelors degree pref in Life sciences or engineering,experience in IVD would be an advantage.10 years experience in Regulatory and Clinical affairs for the international markets on a global scale.medical device experience esential as would some knowledge of clinical studies
Qualifications/Skills Required
Senior Regulatory Affairs Manager
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