This way, you can position yourself in the best way to get hired. ... Assay Development and Screening Novartis Pharmaceuticals Cambridge Senior Administrative Assistant, Human Resources Daiichi Sankyo, Inc. Basking Ridge MORE JOBS LIKE THOSE View more. Keywords: R&D Engineer, EU MDR, new product design, TMV, medical device exp. The resume for a Production Manager begins with a summary of the job seeker's applicable qualifications.Professional experience follows starting with his current role as a Production Manager in a manufacturing setting.This description contains … Support the sales, marketing, business development and account activities including sales visits, events/seminars, To monitor market trends and track competitors' products to help improving the efficiency of the global business growth strategy, Actively participate in relevant scheme owner committees or working groups to ensure SGS maintains influence and exposure in the area, Develop an intimate knowledge of the competition by constantly overseeing competitive activities, To have overall responsibility for the successful management of the MDR ensuring the global operation is efficient and meets the expectations of internal customers (affiliates), external clients, scheme owners and accreditation bodies, Provide advice and support to product specialists and scheme managers on certifications in area of expertise that may have a regulatory challenge, Provide “Technical Sales/Networking” support to the commercial team and promote BSI, Deliver technical reviews and certification scheme management in support of CE marking, Participate in client meetings to facilitate CE marking processes, Provide Medical Device expertise leadership and mentoring in areas of competence to medical devices personnel, A team player good at relationship building internally and externally, Provide in-house and external training for orthopaedic & non active dental medical devices, Issues closing letters to affiliates when product analysis has been performed, Participate on project teams to improve department processes, Responsible for communicating business related issues or opportunities to next management level, Maintains knowledge of Biosense Webster products and their use, Educates field sales force and affiliates in utilization of complaints department for reporting of field complaints, Documents all information according to Biosense Webster policy and EMEA regulatory standards, Responsible for ensuring personal and company compliance with all local and company regulations, policies and procedures, Good computer skills with knowledge of Microsoft Office, Strong verbal and written communication skills, including the ability to make effective and persuasive presentations, Demonstrated ability to work effectively in a highly charged, fluid environment, Very detail-oriented, well-organized, and driven to meet deadlines and program goals, "Combination" Medical Device/Pharma/Disposables Products, A self-starter with the ability to work as a Project Leader managing projects and allocation of resources to those projects, Demonstrated ability to independently manage multiple projects, Demonstrated working knowledge of scientific principles, A degree in Accountancy/Finance and an Accounting Qualification, At least 10 years of working experience in an MNC and in the FMCG/Medical industry, At least 5 years experience in a managerial role, Experience in a Big 4 Auditing firm will be an advantage, Excellent communication skills & business acumen, Provide strategic business perspective to leadership of Development Program team(s) and the evolving program strategy; matrix management of Development Program team, Engagement and communication across franchises and functional lines, including impact on strategic thinking at the Franchise Team and Research and Development Team, Partnership with Program Management (PM) representative on Development Project team to ensure consistent high quality output from the team, and engagement with PM with regard to exploring opportunities to enhance speed and/or project value, Close collaboration with the GDTL for the MPS and MLD programs, Accurate and effective budget management for Development Program(s), addressing issues as they arise, Assessment of Business Development opportunities which could impact on Development Program(s), monitoring external scientific information and competitor activity related to Development Program(s) and modifying project strategy as appropriate, Tracking progress against program goals and composing monthly reports for senior HGT management and HGT/Shire Leadership teams outlining key strategic events for program(s). , strategic imperatives, and validating the prototype of medical devices and companies of ISO... 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