... management, and clinical trials.Lead regulatory submissions, including premarket approvals (PMAs), ... on the business.Participate in regulatory audits and inspections, and drive ... 8 years of experience in regulatory affairs within the medical device ...
... management, and clinical trials.Lead regulatory submissions, including premarket approvals (PMAs), ... on the business.Participate in regulatory audits and inspections, and drive ... 8 years of experience in regulatory affairs within the medical device ...
... management, and clinical trials.Lead regulatory submissions, including premarket approvals (PMAs), ... on the business.Participate in regulatory audits and inspections, and drive ... 8 years of experience in regulatory affairs within the medical device ...
... management, and clinical trials.Lead regulatory submissions, including premarket approvals (PMAs), ... on the business.Participate in regulatory audits and inspections, and drive ... 8 years of experience in regulatory affairs within the medical device ...
... scalable IT systems to support regulatory data requirements. Work closely with ... roles with a focus on regulatory data management, preferably in the ... environment.In-depth knowledge of regulatory standards in the flavor industry, ...
... BSI in stakeholder meetings and regulatory forums (NBCG-MED; EU UK ... decision is documented and signed;Regulatory Lead participates in International Schemes, ... Approval tasks to ensure continuous regulatory compliance and support implementation of ...
... requirements in the overarching global regulatory strategy, and develop risk assessment ... prior relevant experience in pharmaceutical Regulatory Affairs and regulatory procedures (including CP DCP MRP). ...
... matter expert on the HR regulatory requirements impacting the Firm’s EU ... developments, particularly in respect of regulatory change and develop deep knowledge ...
... you will support the Product Regulatory Team with ensuring compliance with regulatory requirements applicable to raw materials ... the EMEAI region against applicable regulatory requirementsSupport the assessment of regulatory status as part of the ...
... accountable for the global regulatory CMC strategy as well as ... Authority interactions meetings as regulatory CMC lead and will perform regulatory CMC expert assessments of in- ... registration Experience in driving regulatory CMC activities and in authoring ...