Strong knowledge of EU Medical Device regulations and guidance documents as well as relevant standards. Experience of Tech File and technical Documentation for submission to notified bodies Ability to work with cross-functional team members including (but not limited to) R&D, Quality, Labelling, Sterility, Medical and Clinical. Experience in working with PLM systems (i.e. Agile and Windchill) Proficient with MS Office applications such as MS Word, PowerPoint, Excel. Excellent communication and inter-personal skills. Ability to manage multiple tasks and be detail-oriented. Experience in coordinating with offshore teams, preferably experience of working with teams in India
Identify reference documents for technical documentation including, but not limited to design and risk documents, verification/validation documents, standards conformance, and labeling. Identify and adhere to policies, procedures and work instructions which support technical documentation activities. Provide support for Clinical Evaluation Reports including references to required documentation. Align technical documentation according to OneMD technical documentation structure proposed by the MDR team. Prepare technical documentation for submission to and reviewed by Notified Bodies, as required. Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regulatory bodies. Maintain information on worldwide regulatory requirements and the status of product registrations. Be responsible for adherence to timelines and ensure milestones are achieved. Report issues to the Customer and Client management to ensure appropriate closure.