Responsibilities: Support the IVDR project by revising the assigned technical files. Each technical file must be generated using the latest technical file template and it must clearly present the product. Must attend multiple weekly meet...
Responsibilities and Requirements: Will primarily be responsible to work on tasks that are routine in nature where limited judgment is required. Receives general instructions on work assignments. Pulls materials from inventory locations....
and prepare other CMC ad-hoc requests as per client requests. Requirements: A Bachelor's degree in a health or life science...
Responsibilities and Requirements: Computer System Validation in addition to validation and regulation experience, the resource should have the following Experience: 3-7 years of relevant experience; can work independently and guide ment...
. Requirements: University Degree (Equivalent to Bachelor's degree) in Chemistry, Biology, Environmental Sciences, Toxicology...
Responsibilities : Work with cross-functional teams to provide regulatory guidance during the development of Class III Medical Devices Establish the regulatory strategy and global registration plan for products, meeting internal quality ...
integration. Requirements: BS or MS in Computer Science or Biostatistics & Life Sciences. Minimum of 7 years of industry...
Responsibilities and Requirements: Configure retirement services products and features within the technology platform to meet business requirements and regulatory standards. Collaborate with stakeholders to define product specifications ...
+ years of Med Device or Life Science Quality Management, or Quality Engineering supporting manufacturing. Some Supervisory...
Responsibilities : Clinical Data Manager, overseeing all deliverables of activities outsourced to DM CRO for multiple studies. Interact and manage relationships with other functional areas to ensure high quality data management activitie...